Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
Login Abbonamenti Pubblicazioni Carrello Registrazione Perché registrarsi? Contatti

Peptide Hormones

140 articoli — 1997-2026 Include sottocategorie MeSH

RI Editoriali
Disforia di genere e dintorni: dieci anni dopo

Tornese G.

2026/3 — pag. 143-144 — DOI

EL I Poster degli specializzandi
Accesso libero
Il bambino con il naso a becco di uccello

Gauci MC, Portale G, di Cataldo G, Leone G, Gambilonghi F, di Nora A, Caruso M

2026/1 — pag. 24-26 — DOI

This report describes the case of an 8-year-old boy presenting with short stature and distinctive facial features, including microphthalmia, a “beak-shaped” nose and mandibular hypoplasia. A clinical diagnosis of Hallermann-Streiff Syndrome (HSS), ch...

RI Problemi correnti
Diagnostica ambulatoriale nella gestione delle infezioni respiratorie acute nelle cure primarie pediatriche

Reggiani L.

2025/9 — pag. 573-582 — DOI

In recent years, the possibility of performing diagnostic tests in the physician’s office (Point of Care) has made countless advances: both in the etiological investigation of viruses or bacteria through pharyngeal or nasopharyngeal swabs or via bloo...

RI Casi indimenticabili
Bassa statura: tutta colpa del papà

Tornese G.

2025/9 — pag. 598-600 — DOI

A child with slow growth and normal hormonal tests shows distinctive physical features. Clinical exome sequencing reveals a mutation in the IHH gene, inherited from the father, who had initially been overlooked. The child responds very well to growth...

EL I Poster degli specializzandi
Accesso libero
Sfide endocrinologiche neonatali: un caso di ipopituitarismo congenito

Carabelli G, Sala Veni C, Cardani R, Salvatore S, Agosti M

2025/7 — pag. 194-195 — DOI

A full-term newborn delivered by urgent caesarean section developed persistent hypoglycemia within the first hours of life, along with hypotonia, poor feeding and prolonged jaundice. Endocrine evaluation revealed congenital hypopituitarism, confirmed...

EL I Poster degli specializzandi
Accesso libero
Diarrea intrattabile e neuroblastoma

Contratto c, Casabona F, Avanzini S, conte M, Gandullia P

2025/5 — pag. 127-128 — DOI

A previously healthy three-year-old girl presented with persistent diarrhoea, progressive abdominal distension and weight loss. After negative infectious and anatomical workup, abdominal imaging (ultrasound, MRI and CT) revealed a retroperitoneal mas...

EL I Poster degli specializzandi
Accesso libero
Un calciatore a cui tremano le gambe: un caso di ipoparatiroidismo

Marchese S, Raso E, Dolce R, Bignone L, Di Bella L, Maggio MC, Corsello G

2024/9 — pag. 193-195 — DOI

The paper presents the case of a 13-year-old athlete who experienced sudden tremors, limb pain, hand spasms and severe hypocalcemia (6 mg/dl). Tests revealed low parathyroid hormone (PTH), hyperphosphatemia and low vitamin D levels. The diagnosis of ...

RI Problemi correnti
L’enuresi notturna: inquadramento e gestione

Renzullo AM, Benvenuto S, Nait G, Pennesi M.

2024/8 — pag. 499-504 — DOI

Enuresis is the involuntary discharge of urine during sleep. It is a fairly common problem in paediatric age: approximately 1 child out of 5 is affected at 5 years of age, with a potential significant impact on their quality of life and family. Patho...

EL I Poster degli specializzandi
Accesso libero
Sembra un deficit di GH, e invece non lo è!

Casini F, Magenes VC, Guida G, Lonoce L, Pozzi E, Cocuccio C, Arrigoni S, Zuccotti G

2024/7 — pag. 142-143 — DOI

A 2.5-year-old girl was evaluated for poor growth. Despite low IGF-1 levels, GH deficiency was excluded. Further investigation revealed celiac disease, diagnosed via EGDS. After starting a gluten-free diet, catch-up growth was observed. The patient r...

EL I Poster degli specializzandi
Accesso libero
Una pubertà che brucia le tappe

Solidoro S

2024/26 — pag. 3-3 — DOI

The diagnosis of idiopathic central precocious puberty was eventually made in an 8-year-old boy with increased testicular volume and growth rate in the absence of bone age advancement based on an elevated baseline LH level. ...

RI Farmacoriflessioni
I LAGH (ormoni della crescita long-acting): cosa sono e a chi proporli?

Rodaro C, Tornese G.

2024/6 — pag. 371-375 — DOI

Children with growth hormone deficiency are currently treated with daily injections of recombinant growth hormone. The burden of 365 injections per year and cold chain storage causes a poor medication adherence. Long-acting growth hormones were devel...

RI Lettere
Quando la pertosse riemerge: si discute del noto e non noto

Parisi M, Marchetti F.

2024/5 — pag. 284-285 — DOI

RI Casi indimenticabili
C'è rachitismo... e rachitismo

Trombetta A.

2024/2 — pag. 119 — DOI

The cases of two adolescents finally diagnosed as affected by two different types of Rickets are presented and discussed...

EL Caso contributivo
Un caso di ipopituitarismo in età infantile

Guida M, Malizia G, Ferrara D

2023/8 — pag. 146-150 — DOI

Hypopituitarism is often an evolutionary condition, which if not present at birth with the classic signs of severe hypoglycaemia, prolonged jaundice, bilateral cryptorchidism and / or micropenis and alterations of neurological development, causes a d...

EL Il punto su
Disfunzioni tiroidee "mascherate" all’interno dei range di normalità

Canali G, Garella V, Taranto S, L’Assainato S, Calcaterra V, Zuccotti G

2023/7 — pag. 125-129 — DOI

Thyroid function plays a crucial role in metabolic homeostasis, in the regulation of blood pressure, energy expenditure and in glucose and lipid metabolism. Thyroid alteration patterns, particularly hypothyroidism, are widely known to be associated w...

RI Problemi speciali
Ipotiroidismo subclinico: realtà e falsi miti

Burlo F, Tonetto S, Tamaro G, Faleschini E, Tornese G.

2023/6 — pag. 369-373 — DOI

Subclinical hypothyroidism (SH or hyperthyrotropinemia) is a biochemical condition defined as elevated serum TSH concentrations and normal thyroxine (FT4). Generally, it is asymptomatic and is distinguished in mild (TSH between the upper limit and 9....

RI Problemi speciali
Disordini tiroidei nel bambino e nell’adolescente con trisomia 21

Molinari S, Fossati F, Gazzarri A, Lazzerotti A, Barzaghi S, Ocello L, Grimaldi C, Nicolosi ML, Biondi A, Cattoni A.

2023/6 — pag. 374-380 — DOI

Thyroid function disorders are the most frequently detected medical complication among patients with trisomy 21, with a reported prevalence ranging from 4-8% in childhood to 50% or more in adulthood. Over 1% of newborns with Down syndrome show clinic...

EL Caso contributivo
Fisiopatologia dell’ipotiroidismo acquisito

Folegatti A, Cardani R, Vergori A

2023/5 — pag. 82-86 — DOI

Acquired hypothyroidism represents a frequent challenge for paediatricians. Knowing the pathophysiological basis of this disease and its main clinical manifestations is closely linked to proper diagnostic and therapeutic management. As is well known,...

RI Casi indimenticabili
Ipoglicemia in un neonato e iperinsulinismo

Risso FM, Tornese G.

2022/1 — pag. 56-58 — DOI

The authors describe the case of a newborn with hyperinsulinemic hypoglicemia due to a genomic variant, with paternal segregation, in ABCC8 gene. The therapeutic and prognostic implications are discussed...

EL Ricerca
Accesso libero
Affinché non MIS-Cappi il caso: l’esperienza di Palermo sulla sindrome infiammatoria multisistemica SARS-CoV-2-correlata

Giordano S, Pirrone I, Restivo GA, Collura F, Saia GF, Maggio MC, Finazzo F, Failla MC, Colomba C, Siracusa L

2021/10 — pag. 289-297 — DOI

Background - Covid-19 is less frequent and milder in children than in adults. However, cases of multisystem inflammatory syndrome temporally associated with SARS-CoV-2 (MIS-C) have been reported in children, whose phenotype resembles atypical Kawasak...

RI Casi indimenticabili
Una mano da SHOX

Bossini B, Pellegrin MC

2021/8 — pag. 525-526 — DOI

A gene SHOX haploinsufficiency was diagnosed in a 13-year-old girl with short stature. Madelung deformity was absent but some dysmorphism of the fingers and toes were present....

RI Speciale
Endocrinologia e diabete

Chiarelli F, Faleschini E, Tornese G

2021/26 — pag. 4 — DOI

RI Aggiornamento
Decifrare la bassa statura nei bambini

Chiarelli F, Castorani V, Polidori N

2021/3 — pag. 159-166 — DOI

Short stature is the most common cause of referral to paediatricians. Only a minority of children with short stature have an underlying pathology. Although well-established diagnostic and management paradigms do exist, recent advances in molecular te...

EL I Poster degli specializzandi
Accesso libero
Alla conquista della sindrome di West

S. Rosati, S. Di Marco, M. Valiani, A. Bonuccelli, D. Peroni

2020/10 — pag. 260-260 — DOI

The paper presents the cases of two infants affected by the so-called West syndrome. Despite a classical clinical presentation in one of the two cases, the diagnosis was delayed because of a previous erroneous diagnosis of gastroesophageal reflux dis...

EL Caso contributivo
Anemia normocitica e dosaggio degli ormoni tiroidei

E. Ferretti, C.M. Pini, L. Luti

2020/9 — pag. 228-230 — DOI

The paper describes the case of an 11-year-old girl presenting with normocytic hyporegenerative anaemia associated with increase of transaminases, CK and LDH. On physical exam skin pallor, mask-like facies and dry skin were observed; weight and heigh...

RI Casi indimenticabili
Poco reattiva… in tempi di pneumococchi cattivi

M.E. Liverani, C. Ziparo

2020/8 — pag. 531-532 — DOI

EL I Poster degli specializzandi
Accesso libero
Thelarche variant: a metà tra telarca prematuro e pubertà precoce

S. Contorno

2019/10 — pag. 247-247

RI Problemi speciali
Bassa statura da deficit di gene SHOX: vecchi e nuovi concetti

M.C. Pellegrin, S. Andrade, E. Faleschini, E. Barbi, C. Bizzarri, G. Tornese

2019/7 — pag. 438-444

At the moment alterations of SHOX gene, located in the pseudoautosomal region of sex chromosomes, are considered the most frequent genetic defects associated with short stature. Pathogenic mutations leading to SHOX deficiency involve not just exons...

RI Aggiornamento
Corto come il papà

G. Tornese

2019/7 — pag. 431-437

Familial short stature is the second cause of short stature immediately after constitutional delay of growth and puberty. So far, in case of familiarity for short stature, regular growth velocity, bone age compatible with chronological age, the ind...

EL I Poster degli specializzandi
Accesso libero
Una bambina piccola con le dita coniche

V. Carrato, A.G. Grasso

2019/7 — pag. 154-154

RI Aggiornamento
Ma che fine fanno gli SGA?

G. Tornese

2019/6 — pag. 355-364

Recombinant human growth hormone (rhGH) is an approved and effective treatment for short children born small for gestational age (SGA). Prevalence of children eligible for treatment as SGA is reported to be 1:1,800. The latest data from the Italian...

RI Percorsi clinici
Pubertà precoce da causa organica

M. Cozzolino, A. Zucchini, F. Marchetti

2019/4 — pag. 243-246

The paper describes a case of a child with rapidly progressive central puberty (PPC) secondary to hypothalamic hamartoma. Hypothalamic hamartoma is a congenital malformation diagnosed with MRI. It may be associated with PPC, gelastic seizures and m...

RI Aggiornamento
Sovrappeso ma non solo: come riconoscere le obesità sindromiche

M. Ferrario, P. Cianci, A. Bosco, A. Selicorni

2019/4 — pag. 223-230

Obesity is a complex and multifactorial disease resulting from the interaction between genes and environment. The increasing prevalence of obesity in paediatric age needs a reasoned approach to obese children and the identification of also less fre...

EL I Poster degli specializzandi
Accesso libero
Complicanze endocrinologiche nei bambini affetti da neurofibromatosi 1 e glioma delle vie ottiche

M. Scilipoti

2019/4 — pag. 93-93

RI Pagine elettroniche
L’adolescente obeso: è importante valutare i genitali

B. Mainetti, M.T. Nasi, E. Valletta

2018/9 — pag. 595-596

The article describes the case of an adolescent male with obesity and pubertal delay whose hormonal and imaging investigations led to the diagnosis of prolactin secreting pituitary adenoma. After cabergoline treatment, a decrease in prolactinoma size...

RI Aggiornamento
Sarà maschio o femmina?

L. Lucaccioni, A. Boncompagni, E. Pietrella, P.L. Ceccarelli, F. Ferrari, A. Berardi, L. Mughetti

2018/9 — pag. 561-568

After the first trimester of pregnancy future parents are commonly asked if their child will be male or female. Such a question creates many expectations and implies the true determination of the baby's identity. Indeed, since the earliest stages of ...

EL Il punto su
Diabete tipo 1 e malattie intercorrenti: domande e risposte

V. Graziani, T. Suprani

2018/7

RI Casi indimenticabili
Una cefalea importante

G. Acucella, E. Eljerbi, G. Grugni, A. Guala

2018/3 — pag. 192-193

RI Articolo speciale
Disforia di genere e dintorni

G. Tornese, M. Di Grazia, A. Roia, G. Morini, D. Cosentini, M. Carrozzi, A. Ventura

2016/7 — pag. 437-444

Gender identity is a dimension of sexual identity and refers to persistent personal conception of oneself as male or female. Gender identity development is not always in accordance with the biological sex, therefore - even from an early age - some ...

RI Pagine elettroniche
Chetoacidosi secondaria a tireotossicosi in ragazza con diabete tipo 1 e celiachia

V. Graziani, A. Zucchini, T. Suprani, F. Currò, L. Mambelli, F. Marchetti

2016/3 — pag. 191-194

The paper describes the case of a teenager affected by type 1 diabetes mellitus and coeliac disease who presented secondary ketoacidosis (DKA) triggered by thyrotoxicosis. She was successfully treated with beta-blocker and methimazole, in addition...

EL Casi indimenticabili
Le crisi gelastiche

C. Pierobon, D. Driul, G. Crichiutti

2016/3

RI Organizzazione sanitaria
Accesso libero
Il bambino con diabete a scuola: l’autonomia comincia con la maestra

V. Graziani, T. Suprani, M. Marsciani, M. Farneti, A. Faetani, T. Piscone, M.R. Ghinassi, G. Monti, E. Ravaioli, A. Biasini, F. Marchetti

2015/10 — pag. 644-651

The management of insulin-dependent diabetes in young children is challenging and, despite the availability of technological devices, these children need assistance or supervision by an adult to perform blood monitoring and insulin administration a...

RI Editoriali
Il diabete che fa scuola

M. Pocecco

2015/10 — pag. 619-620

RI Problemi speciali
Ipopituitarismo congenito

P. Matarazzo, M. Repici, A. Ravaglia

2015/7 — pag. 452-457

A lot of genes govern pituitary gland development, differentiation and function. Mutations in those genes, as well as toxic or infective intrauterine noxae, could derange pituitary gland development, differentiation and function. More precocious is...

EL I Poster degli specializzandi
Accesso libero
Ipogonadismi, terapia ormonale sostitutiva dello sviluppo puberale

G. Tornese, E. Conversano

2015/7

EL I Poster degli specializzandi
Accesso libero
Un caso particolare di pubertà precoce

P. Scalini, M. Giacalone, S. Ricci

2015/6

RI L'esperienza che insegna
L’ipoglicemia da iperinsulinismo: la diagnosi, le cause, la gestione

F. Marchetti, V. Graziani, M. Cappella, G. Vieni, C. Muratori, T. Tosi, M. La Bianca, F. Faletra

2014/5 — pag. 309-314

The paper describes the case of a 3-month-old girl with seizures due to persistent nonketotic hypoglicaemia with moderate iperammoniaemia. Once tyrosinemia, urea cycle disorders, deficit of fatty-acids-beta-oxidation and other organic acidurias had...

RI Rubrica iconografica
Una tumefazione del clitoride

V. Graziani, M. Mainetti, F. Currò, S. Dal Bo, P. Ghetti, A. Zucchini, F. Marchetti

2014/2 — pag. 113-115

RI Aggiornamento
La gestione del bambino con diabete di tipo 1

T. Suprani, V. Graziani, A. Cirillo, A. Biasini, F. Marchetti

2014/2 — pag. 87-95

The primary objective in type 1 diabetes management is the maintenance of good metabolic control in order to reduce the incidence of acute adverse events and long term complications. Recently, thanks to technological advances, use of new insulin an...

EL Caso contributivo
Vitamina D: è indispensabile... ma non esageriamo!

E.M.G. Marrella, S.Tagliati, S. Brachi, C. Gelli, M. Giovannini, G. Turlà, C. Malaventura

2013/8

The article presents a case of severe hypercalcemia due to hypervitaminosis D in a 5-month-old infant. The child was fed with infant formula. He received 2 drops of 25-hydroxy vitamin D3/day since he was born. His clinical features showed growth reta...

EL I Poster degli specializzandi
Accesso libero
Uno strano caso di enuresi

T. Timpanaro, P. Barone, R. Garozzo

2013/7

RI Percorsi clinici
Pubarca precoce, irsutismo, amenorrea e bassa statura: quale diagnosi?

A. Zucchini, F. Marchetti

2013/1 — pag. 35-38

Non-classical congenital adrenal hyperplasia (NCCAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms. The article reports a case of NCCAH due to 21-hydroxylase deficiency in a 14-year-old girl with prem...

EL I Poster degli specializzandi
Accesso libero
Troppa acqua non fa crescere

S. Naviglio, M.C. Pellegrin, G. Patti

2012/7

RI Problemi speciali
Il deficit del gene SHOX come causa di bassa statura

L. Iughetti, S. Bernasconi, E. Caruso-Nicoletti, F. Chiarelli, A. Cicognani

2011/6 — pag. 367-373

SHOX gene (Short Stature Homeobox-containing gene) seems to play an important role in the growth process. Indeed, patients with mutations or deletions of this gene present with variable degrees of stature deficiency that in the most serious cases i...

RI Aggiornamento
Uno, cento, mille diabetiDiabete mellito di tipo 1 e 2 - parte prima

G. Tornese, L. Rubert, G. Tonini, E. Faleschini

2011/6 — pag. 360-366

The term “diabetes mellitus” does not only refer to one disease, but to a group of metabolic diseases characterized by chronic hyperglycemia resulting from defects in insulin secretion, action, or both. The vast majority of cases of diabetes falls in...

RI Consensus
Uso degli analoghi del GnRH nei bambini

F. Chiarelli, E. Conte

2010/7 — pag. 435-445

The development of Gonadotropin Releasing Hormone analogs (GnRHa) revolutionized the treatment of central precocious puberty (CPP). However, questions remain regarding their optimal use in CPP and other conditions in children. The European Society ...

RI Ricerca
La gestione del bambino con testicolo ritenuto

F. Marchetti, L. Ronfani, J. Bua, G. Tornese, G. Piras, G. Toffola nome del Gruppo di Studio italiano sul testicolo ritenuto

2010/4 — pag. 250-258

Background: The aims of our study were to describe the current management of cryptorchidism among Italian family paediatricians (FP) and detect any difference from the recently published Nordic Consensus guidelines. Methods: An online questionnair...

RI Consensus
Linee guida sulla diagnosi e il trattamento del bambino con bassa statura idiopatica

F. Chiarelli, R. Salomone

2008/10 — pag. 626-633

ISS is defined auxologically by a height below -2 SDS without findings of disease after a complete evaluation by a pediatric endocrinologist (including bone age X-ray, thyroid function, karyotype for girls, and measurements of IGF-I and stimulated gr...

RI Consensus
Gestione della sindrome di Turner in età pediatricae durante la vita adulta

R. Salomone, F. Chiarelli

2008/3 — pag. 157-165

This consensus statement arose from an interdisciplinary meeting of geneticists, paediatricians, cardiologists, internists, behavioural health specialists, and gynaecologists involved in the care of and clinical research on patients with Turner Syn...

RI Consensus
Il trattamento del testicolo ritenuto

E. Conte, F. Chiarelli

2007/9 — pag. 573-579

In August 2006 a group of specialists in testicular physiology, paediatric surgery/urology, endocrinology, pathology and anaesthesiology convened for two days in Sigtuna (Sweden) to allow preliminary conclusion of the most controversial issues in the...

EL Pediatria per l'ospedale
Accesso libero
Fisiopatologia della vitamina D (Prima parte)

G. Bartolozzi

2007/9

RI Pagine elettroniche ; Caso Contributivo
Ipertensione endocranica idiopatica (pseudotumor cerebri) in una bambina in terapia con ormone della crescita

G. Tornese, F. Patarino, S. Pensiero, F. Parentin, E. Faleschini, G. Tonini, F. Marchetti

2007/7 — pag. 459-461

We report a case of idiopathic intracranial hypertension (IIH) (pseudotumor cerebri) following treatment with recombinant growth hormone (rhGH). A 9-year-old girl, treated for GH deficiency, developed bitemporal worsening headache, diplopia, intermit...

EL Contributi Originali - Casi contributivi
Accesso libero
Ipertensione endocranica idiopatica (pseudotumor cerebri) in una bambina in terapia con ormone della crescita

G. Tornese, F. Patarino, S. Pensiero, F. Parentin, E. Faleschini, G. Tonini, F. Marchetti

2007/7

RI Consensus
Il bambino nato piccolo per l’età gestazionale

R. Salomone, F. Chiarelli

2007/6 — pag. 363-369

Being small for gestational (SGA) leads to consequences not only in the neonatal period but also in adulthood. During the last 15 years, a number of long term risks of being SGA have been clearly identified, including hypertension, ischaemic heart ...

EL Pediatria per l'ospedale
Accesso libero
Il parto (Parte prima)

G. Bartolozzi

2007/3

RI Consensus
Consensus statement sulla chetoacidosi diabetica nei bambini e negli adolescenti

S. Di Michele, F. Chiarelli

2007/1 — pag. 19-25

Background. Diabetic Ketoacidosis (DKA) is the leading cause of morbidity and mortality in children with Type 1 Diabetes Mellitus (TIDM). Mortality is predominantly related to the occurrence of cerebral oedema; only a minority of deaths in DKA are ...

RI Pagine elettroniche ; Caso Contributivo
Segnalazione di un caso di diabete neonatale

G. Dioguardi, G. Ricciardi, G. Micelisopo, A. Gallo, AM. D’Antonio, M. De Vivo, A. Palermo

2006/4 — pag. 257-258

Detection of diabetes during neonatal age is very infrequent. Nonetheless early diagnosis is crucial since if not promptly treated with insuline, neonatal diabetes (ND) has a critical course. We report the case of a female neonate, born with birth w...

EL Caso Clinico Interattivo
Accesso libero
Una bambina con polipnea

M. Londero, S. Minisini, E. Faleschini, G. Messi, E. Barbi

2006/4

EL Appunti di Terapia
Accesso libero
L'adeno-tonsillectomia fa ingrassare?

G. Bartolozzi

2006/3

EL Contributi Originali - Ricerca
Accesso libero
La prescrizione di farmaci soggetti a nota nella popolazione pediatrica italiana.

S. Maschi, A. Clavenna, E. Rossi, A. Berti, M. De Rosa, M. Bonati

2005/7

RI Pagine elettroniche
La prescrizione di farmaci soggetti a Nota nella popolazione pediatrica italiana

S. Maschi, A. Clavenna, E. Rossi, et al.

2005/7 — pag. 475-477

The objectives of the study are to evaluate the pattern of drug prescriptions reimbursed with limitations (AIFA notes) by the National Health System in the Italian paediatric population. Prescriptions involving 982,035 children ...

EL Seminari degli specializzandi
Accesso libero
L'ipotiroidismo dalla nascita in poi

I. Berti, I. Giuseppin, R. Meneghetti

2005/3

RI Problemi non correnti
Ipotiroidismo subclinico: dalla teoria alla pratica

C. Locatelli, M. Bensa, M. Pocecco

2005/3 — pag. 165-168

Subclinical hypothyroidism is a biochemical state characterized by an elevated serum TSH level with concomitant normal FT4 value. While in adults it frequently progresses to clinically evident hypothyroidism, in children it may be a benign and remi...

EL Pediatria per l'ospedale
Accesso libero
Emofilia A e B2° parte

G. Bartolozzi

2005/1

RI Digest
Le basi molecolari dell’obesità

2005/1 — pag. 44-45

EL Seminari degli specializzandi
Accesso libero
Quando dare la vitamina D

S. Bassanese, S Norbedo

2004/8

RI Aggiornamento
La pubertà precoce

S. Cianfarani

2004/8 — pag. 485-491

Precocious puberty is a condition that has both physical and psychological effects on affected children and their families. Therefore, an accurate work up is necessary to understand the dynamic course of the disease in terms of rate of pubertal pro...

EL Seminari degli specializzandi
Accesso libero
Protocollo in caso di sviluppo puberale precoce

a cura di G. Tonini, E. Faleschini, G. Borotto, I. Giuseppin

2004/1

EL Seminari degli specializzandi
Accesso libero
Puberta' precoce, pseudopuberta' e affini

E. Faleschini, G. Borotto, I. Giuseppin

2003/10

EL Caso Clinico Interattivo
Accesso libero
Diabete insulino-dipendente in fase di cattivo controllo

M. Lazzerini

2003/9

EL Caso Clinico Interattivo
Accesso libero
Diabete insulino-dipendente in fase di cattivo controllo

M. Lazzerini

2003/9

EL Caso Clinico Interattivo
Accesso libero
Diabete insulino-dipendente in fase di cattivo controllo

M. Lazzerini

2003/9

RI Casi indimenticabili
Maria... sei anni dopo

F. Fusco

2003/8 — pag. 532-534

EL Avanzi
Accesso libero
Necessità di un supplemento di vitamina D negli allattati al seno

G. Bartolozzi

2003/8

EL Caso Clinico Interattivo
Accesso libero
La storia di Tina

M. Lazzerini

2003/7

RI Controversie
Accesso libero
Enuresi e desmopressina

M.L. Chiozza, M. Pennesi, L.Peratoner

2002/5 — pag. 318-322

WHY SHOULD WE USE IT? The Author underlines that disturbances in three different areas (sleeping quality, bladder maturity and diuresis control) concur to the the pathogenesis of enuresis.Therefore the case management should take all of them into ...

RI Domande e risposte
Accesso libero
Domande e risposte

G. Longo

2002/1 — pag. 58-59

RI Aggiornamento monografico
Accesso libero
La pubertà femminile: come e quando esordisce, con che ritmo procede, quando intervenire

S. Di Maio

2002/1 — pag. 20-26

Over the last century there has been a trend to earlier onset of female puberty and a great variability of the age of onset has been observed. A tendency towards a slower pubertal development, particularly in cases at earlier onset, has also been o...

RI Aggiornamento monografico
Accesso libero
Il diabete insipido centrale: più luci e meno ombre

M. Maghnie

2001/6 — pag. 361-368

Diabetes insipidus is a multifactorial disease caused by the lack of secretion of vasopressin, its physiologic suppression following excessive water intake, or kidney resistance to its action. The clinical and laboratory diagnosis is confirmed by s...

RI Aggiornamento monografico
Accesso libero
L’enuresi notturna

M.C. Mencoboni

2000/9 — pag. 565-570

Enuresis is a very frequent complaint: its prevalence is 10% in 6-year old children. Primary nocturnal enuresis is a multifactorial condition, where an unbalance between urine production and bladder functional capacity is associated with arousal pr...

RI Pagina verde
Accesso libero
Eritromelalgia, vasculite, vitiligo, ipertensione, difetto di gh

R. Cimaz, A. Langer

2000/6 — pag. 391-393

Description of a case of idiopathic erythromelalgia, started at about 5 years, which dramatically developed over many years, with painful crises to the feet (and then also to the hands) mitigated in cold conditions only, with trophic alterations t...

RI L'angolo dell'immunologo
Accesso libero
Il diabete visto dall’intestino

A. Tommasini et al.

2000/4 — pag. 253-258

RI Problemi correnti
Accesso libero
Elogio dei ricostituenti

A. Brunelli

1999/10 — pag. 627-628

RI Problemi correnti
Accesso libero
Calendario chirurgico

A. Messineo

1999/10 — pag. 627-628

The timing and treatment of a few common surgical conditions are discussed. Inguinal hernia should be surgically treated as soon as possible. Funicular cyst and hydrocele can wait until the end of the second year. Testes must be in their scrotal si...

RI Aggiornamento monografico
Accesso libero
Vescica instabile ed enuresi

L. Peratoner

1999/10 — pag. 623-625

Immature bladder is a physiologic condition in infants and toddlers. In the great majority of cases, nocturnal enuresis is accompanied by signs of immature bladder (urgency, frequency, day incontinence etc.) during daytime. Treatment with alarm dev...

RI Aggiornamento monografico
Accesso libero
L’ipotiroidismo congenito

G. Tonini, M. Lazzerini

1999/8 — pag. 481-488

The incidence of Primary Congenital Hypothyroidism (PCH) is about 1:2000. Most cases are due to a dysgenetic/ectopic thyroid. Only in a small minority of cases a defect in the iodine metabolism is present. Congenital hypothyroidism secondary to a d...

EL Appunti di Terapia
Accesso libero
L'insulina aspart

G. Bartolozzi

1999/7

EL Il punto su
Accesso libero
Il diabete insipidoIl bilancio dell'acqua

G. Bartolozzi

1999/6

RI Linee guida
Accesso libero
Schemi e dosi di terapia insulinica nel bambino diabetico

M. Pocecco

1999/2 — pag. 113-115

RI Linee guida
Accesso libero
Indicazioni all’uso dell’ormone della crescita

M. Pocecco

1998/8 — pag. 541

RI Problemi correnti
Accesso libero
Iponatremia da trattamento con DDAVP: la desmopressina e l’enuresi notturna

P.P. Molinari, A. Lambertini, G. Giovannini e coll.

1998/4 — pag. 227-228

Desmopressin (DDAVP) is widely used in the treatment of primary nocturnal enuresis. It is a safe and effectiv drug, but occasionally water intoxication may occur. We report a 5 - year - old girl who developed generalized seizures due to hyponatr...

RI Editoriali
Accesso libero
Incompetenza, confusione, fanatismo

M&B

1998/1 — pag. 8

RI Novità
Accesso libero
Novità in Pediatria pratica 1996-1997

F. Panizon

1997/10 — pag. 649-674