Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Lipids

89 articoli — 1998-2025 Include sottocategorie MeSH

EL Caso contributivo
Infezioni rare del flusso sanguigno correlate a catetere: coinvolgimento insolito di batteri tipicamente non patogeni in un caso pediatrico. Come trattare?

Barbera G, La Malfa G, Saia GF, Cardillo M, Sanfilippo MF, Comparato C

2025/10 — pag. 260-263 — DOI

Rothia dentocariosa, a commensal organism of the oral cavity, is an uncommon pathogen that predominantly affects immunocompromised individuals or patients with indwelling medical devices. The paper reports a case of Rothia dentocariosa catheter-relat...

RI L'aria che tira
Allarmi alimentari: la lobby della paura

Defez R.

2024/9 — pag. 583-584 — DOI

Food product advertising bombards the consumer with alarming information and tends to blame them, by making them responsible for putting their children, grandchildren and relatives at risk when purchasing products that ignore the warnings of advertis...

EL I Poster degli specializzandi
Accesso libero
Prima l'epatite autoimmune e poi la MICI... dopo tanto tempo

Izzo BP, Mainetti M, Aprile MR, Foschi F, Buzzi A, Marchetti F

2024/26 — pag. 4-5 — DOI

The authors describe the case of a girl with IBD that manifested 10 years after the diagnosis of seronegative hepatitis. ...

RI Casi indimenticabili
L’epilessia mioclonica giovanile

Colussi L.

2023/7 — pag. 462-463 — DOI

The diagnosis of myoclonic epilepsy was eventually made in an adolescent girl who presented with generalized convulsions after a night at the disco....

RI Pagine elettroniche
Lesioni ossee simmetriche e drepanocitosi

Franzone D, Chianucci B, Basso L, Guardo D, Bellini T, Piccotti E.

2023/6 — pag. 399-402 — DOI

An 8-year-old boy suffering from sickle cell disease (SCD) was admitted to emergency unit complaining of moderate-to-severe pain in his lower limbs. He received chronic transfusion therapy and hydroxyurea. Apparently, he had never experienced vaso-oc...

RI Aggiornamento
Malattia grassa del fegato: tra fattori ambientali e predisposizione genetica

Mosca A, Maggiore G.

2023/6 — pag. 355-362 — DOI

Non-alcoholic fatty liver disease (NAFLD) is now recognized as the hepatic manifestation of the metabolic syndrome and is the most common cause of chronic liver disease in both adults and children. It is assumed that a genetic predisposition associat...

EL I Poster degli specializzandi
Accesso libero
Quando la rabdomiolisi risponde al glucosio

Di Nora A, La Spina L, Meli C, Ruggieri M

2023/5 — pag. 91-91 — DOI

The case of an 8-year-old boy complaining easy tiredness, poor exercise tolerance and high CPK blood level is described. The diagnosis of glutaric aciduria type II was finally made....

EL I Poster degli specializzandi
Accesso libero
Una diagnosi complementare: la C3-glomerulopathy

Amoroso S

2022/6 — pag. 134-134 — DOI

The case of a 10-year-old boy with macrohaematuria is presented. The diagnosis of C3-glomerulopathy was eventually made. The author remarks the main clinical and diagnostic aspects of C3-glomerulopathy....

EL I Poster degli specializzandi
Accesso libero
Che cos’è la linfangectasia intestinale?

Razza R

2022/2 — pag. 57-57 — DOI

The case of a 3-month-old infant with severe malnutrition and protein-losing enteropathy finally diagnosed as congenital intestinal lymphangiectasia is presented. The diagnostic and therapeutic challenges of this intriguing disease are discussed....

RI Farmacoriflessioni
Vitamina D e letteratura: fatti e misfatti

Contorno S, Pecile PA.

2021/10 — pag. 646-649 — DOI

In the last twenty years, the international scientific literature paid particular attention to vitamin D deficiency. Many pathological conditions, like allergy, asthma, cancers, autoimmune, cardiovascular and infectious diseases were attributed to vi...

RI Problemi speciali
Le interferonopatie di tipo I

Tommasini A, Bruno I, Morelli ME, Lepore L

2021/8 — pag. 509-514 — DOI

Type I interferonopathies are autoinflammatory monogenic disorders arising from excessive production of interferons. Some manifestations like chilblains, neurologic involvement, arthritis and lipodystrophy may be shared by several diseases. Measure o...

EL Caso contributivo
La sindrome di Zellweger: un lavoro di squadra

Acquaviva I, Cesaroni E, Siliquini S, Sessa F, Marini C

2021/8 — pag. 233-240 — DOI

A 1-month female infant with hypotonia, feeding difficulties, facial dysmorphic signs, hepatomegaly and seizures was admitted to the neonatal intensive care unit. Brain magnetic resonance revealed regions of cortical dysplasia, diffuse polymicrogyria...

RI Focus
Vitamina D e rachitismo carenziale

A. Agrusti, S. Contorno, I. Bruno, G. Gortani, E. Barbi

2020/7 — pag. 426-429 — DOI

Mouhamed, a 7-year-old boy of African origin, presented with progressive fatigue and difficulty in walking. He was never treated with vitamin D supplementation. The evaluation of his calcium-phosphorus metabolism revealed a myopathy related to severe...

RI Farmacoriflessioni
Cannabis ed epilessia in Pediatria: mito o realtà?

C. Forest, E. Fiumana, R. Faggioli, A. Suppiej, G. Maggiore

2019/5 — pag. 303-309

In recent years, there has been an increasing interest for the use of medical Cannabis in Paediatrics. Several pharmacological properties are attributed to Cannabis by preclinical studies, but the most important application is related to the treatm...

RI Pagine elettroniche
Disartria e strabismo: due sorelle, una dopo l’altra. Ovvero: quando lo streptococco dà ai nervi

F. Galdo, V. Pintabona, M. Bramuzzo, F. Pellegrini, A. Ventura

2018/3 — pag. 194-196

Guillain-Barré syndrome (GBS) may follow infections such as Campylobacter jejuni, cytomegalovirus and Haemophilus influenzae infections. The paper describes two familiar cases of polyneuritis cranialis, an oculopharyngeal subtype of GBS, which appear...

EL Caso contributivo
Disartria e strabismo: due sorelle, una dopo l’altra. Ovvero: quando lo streptococco dà ai nervi

F. Galdo, V. Pintabona, M. Bramuzzo, F. Pellegrini, A. Ventura

2018/3

Guillain-Barré syndrome (GBS) may follow infections such as Campylobacter jejuni, cytomegalovirus and Haemophilus influenzae infections. The paper describes two familiar cases of polyneuritis cranialis, an oculopharyngeal subtype of GBS, which appear...

RI Pagine elettroniche
Glomerulopatia da depositi di C3

S. Amoroso, M. Pennesi, A. Ventura

2018/2 — pag. 119-122

C3-glomerulopathy includes several nephropathy charac-terised by almost only C3 deposits without immunoglobu-lins with a mesangial proliferative or membrano-proliferative pattern on light microscopy. C3-glomerulopathy is determined by a dysregulation...

EL Il punto su
Glomerulopatia da depositi di C3

S. Amoroso, M. Pennesi, A. Ventura

2018/2

C3-glomerulopathy includes several nephropathy charac-terised by almost only C3 deposits without immunoglobu-lins with a mesangial proliferative or membrano-proliferative pattern on light microscopy. C3-glomerulopathy is determined by a dysregulation...

RI Pagine elettroniche
Una morfea pansclerotica: nulla è servito

S. Della Paolera, S. Pastore, M. Minute, M. Rabusin, L. Lepore, A. Ventura

2017/8 — pag. 531-532

The paper presents the case of a 12-year-old boy affected by circumscribed morphea that started with multiple skin lesions on both feet and hands. Despite different therapeutic approaches the disease evolved to an extremely disabling form of panscler...

RI Dermo mail
TricotillomaniaImpetigine

2017/7 — pag. 468

RI Pagine elettroniche
Disordini dello "spettro Zellweger": rara causa di convulsioni e ipotonia nel neonato

G. Stangoni, T. Becchetti, G.M. Campus, A. Fantauzzi, R. Scattoni, A. Zeringyte

2016/9 — pag. 602-604

The paper describes a case of a newborn suffering from severe hypotonia and drug-resistant seizures, who was diagnosed with a “Zellweger spectrum” disease by means of biochemical and enzymatic tests. The “Zellweger spectrum” disorders are a group...

EL Caso contributivo
Disordini dello “spettro Zellweger”: rara causa di convulsioni e ipotonia nel neonato

G. Stangoni, T. Becchetti, G.M. Campus, A. Fantauzzi, R. Scattoni, A. Zeringyte

2016/9

RI Percorsi clinici
La medicina “magica” che ti rimette in piedi

G.I. Baroncelli, G. Laccetta, A. Giannoni, F. Massei

2016/7 — pag. 445-448

Prolonged and exclusive breastfeeding without vitamin D supplements is a main determinant of vitamin D deficiency rickets in children of immigrants living in Italy. Dark skin may be an adjunctive factor for the development of rickets. Early signs a...

RI Pediatria flash
Xantomatosi cerebro-tendinea

P. Pascolo

2016/5 — pag. 310-312

RI Farmacoriflessioni
Tramadolo: valida alternativa alla codeina?

A. Di Sessa, P. Marzuillo, L. Calligaris, I. Rabach, S. Furlan, E. Barbi

2016/1 — pag. 41-45

In June 2013, the European Medicine Agency (EMA) prohibited the use of medicines containing codeine for patients under 12 years of age. The EMA recommendations impose a change in the management of moderate-severe pain in children. Tramadol, an opi...

RI Pagine elettroniche
Quali malattie sono legate al deficit di vitamina D?

V. Murgia

2015/8 — pag. 531-532

EL Appunti di Terapia
Quali malattie sono legate al deficit di Vitamina D?

V. Murgia

2015/8

RI Casi indimenticabili
Ma che gambe...!

F. Santoro

2014/8 — pag. 531-532

EL Il punto su
La gestione del bambino con ipercolesterolemia familiare

G.G. Viviano

2014/2

Among hypercholesterolaemias, familial hypercholesterolaemia is a hereditary dyslipidaemia characterised by an isolated and permanent increase in circulating low-density lipoprotein (LDL) levels. The heterozygous form is often clinically silent and m...

RI Pagine elettroniche
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 — pag. 530-531

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 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...

RI Ricerca
Pancreatiti acute e ricorrenti in pediatria: chi, come e perché

F. Minen, A. De Cunto, S. Martelossi, A. Ventura

2013/5 — pag. 302-307

Background - Etiologies of acute pancreatitis in children are more variable than in adults and have different causes. Aims - The aims of this study were: 1) to assess the etiological factors of acute and recurrent pancreatitis in a paediatric popu...

RI Pagine elettroniche
Una strana dermatite dell’area del pannolino: quando lavare troppo fa male

F. Savoia, G. Gaddoni, A. Patrizi, P. Sgubbi

2012/8 — pag. 533-534

The case of a 3-month-old boy that was visited because of a brownish, hyperkeratotic and slightly desquamative dermatitis of the inguinal folds, perineum and perianal area is reported. The patient was healthy, asymptomatic and the remaining physical ...

EL I Poster degli specializzandi
Accesso libero
Un insolito braccialetto

L. Matarazzo

2012/3

EL I Poster degli specializzandi
Accesso libero
Deficienza di vitamina D: un problema “familiare” al pediatra

F. Vierucci, M. Gori, A. Petracchi, G. Carlone, M. Del Pistoia, G. Federico, G. Saggese

2012/3

EL Caso contributivo
Incremento delle transaminasi in un bambino con ipofibrinogenemia congenita e ipobetalipoproteinemia famigliare

M. Fornaro, E. Valletta

2012/1

The article reports the case of a 32-month child, born at the 28th week of gestational age, with a slight persistent increase in AST and ALT since the 11th month of age, hypofibrinogenemia and initial growth delay. Investigations excluded common caus...

EL Casi indimenticabili
È tutto sua mamma!

C. Tuoni, F. Dini, F. Vierucci, G.I. Baroncelli, P. Ghirri, A. Boldrini

2011/8

RI Percorsi clinici
Una bambina con scarsa crescita e segni clinici di rachitismo all’età di 2 anni

S. Pastore, F. Marchetti

2011/5 — pag. 301-305

This work describes the case of a 5-year-old girl who started showing clinical features typical of rickets at the age of 2. Nutritional deficiency rickets was diagnosed although vitamin D implementation therapy did not sort any improving effect. A ...

RI Il commento
Vitamina D, tra dato di laboratorio e salute

F. Panizon

2010/4 — pag. 246-249

RI Problemi correnti
Apporti consigliati di vitamina D: un "ritorno al passato"

G.I. Baroncelli, F. Vierucci, S. Bertelloni, T. Vanacore, G. Vierucci

2010/4 — pag. 237-245

The last guidelines of the American Academy of Pediatrics for prevention of vitamin D deficiency in infants, children, and adolescents recommend a minimum daily intake of 400 IU of vitamin D beginning soon after birth. All breastfed and partially b...

EL Casi indimenticabili
Una sera come tutte le altre!

A. Marzano

2010/4

RI Pediatria flash
Lo stafilococco e l'eczema nummulare

2010/1 — pag. 54

EL Pediatria per l'ospedale
Accesso libero
Lo screening dei lipidi e delle lipoproteine in pediatria (parte seconda)

G. Bartolozzi

2008/8

EL Pediatria per l'ospedale
Accesso libero
Lo screening dei lipidi e delle lipoproteine in pediatria (Parte prima)

G. Bartolozzi

2008/7

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

G. Bartolozzi

2008/1

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

G. Bartolozzi

2007/10

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

G. Bartolozzi

2007/9

EL Casi indimenticabili
Accesso libero
Una ragazza a scatti

D. Giglia

2007/3

EL Appunti di Terapia
Accesso libero
Il celecoxib per la prevenzione degli adenomi sporadici del colon-retto

G. Bartolozzi

2006/9

EL Pediatria per l'ospedale
Accesso libero
ß-talassemia (Parte prima)

G. Bartolozzi

2006/1

RI Aggiornamento monografico
Trattamento della sindrome nefrosica idiopatica corticosensibile

C. Romanello

2005/9 — pag. 580-586

The steroid treatment of Idiopathic Nephrotic Syndrome (ISN) should be continued for at least 3 months, as there is evidence of an inverse correlation between the duration and the total dosage of steroids and the risk of relapses. The tendency to r...

RI Digest
Recettori Toll-like

2005/8 — pag. 544

RI Problemi correnti
L’impetigine

A. Lenhardt, J. Bua, F. Marchetti

2004/11 — pag. 695-698

As a rule bollous impetigo is caused by Staphylococcus aureus. Non bullous, or contagious, impetigo is also caused by Staphylococcus aureus, less frequently by its association with Streptococcus pyogenes. Controlled studies showed that topical anti...

EL Il punto su
Accesso libero
L'epilessia (iv° parte)

M. Lazzerini

2004/8

RI Aggiornamento
Le urgenze cardiologiche in età perinatale Parte I

U. Vairo, et al.

2004/4 — pag. 225-234

Congestive heart failure (CHF) is a clinical syndrome in which the heart is unable to pump enough blood to the body to meet its needs, to dispose of venous return adequately, or a combination of the two. CHF in the newborn usually result from conge...

EL Seminari degli specializzandi
Accesso libero
I FANS in pediatria: dalla teoria alla pratica

T. Gerarduzzi, E. Neri, A. Gagliardo, S. Minisini

2003/9

RI Domande e risposte
Accesso libero
Domande e risposte

G. Longo

2002/4 — pag. 261-262

RI Farmacorecensioni
Accesso libero
Ibuprofene in Pediatria

F. Marchetti

2001/6 — pag. 387-391

EL Contributi Originali - Casi contributivi
Accesso libero
Ittero neonatale e malattia di Nieman-Pick tipo C

C. Martini

2000/10

RI Novità
Accesso libero
Novità in Pediatria pratica 1999-2000

F. Panizon

2000/10 — pag. 647-659

RI Digest e superdigest
Accesso libero
Il latte materno e i suoi assi nella manica

2000/8 — pag. 527-529

RI Problemi correnti
Accesso libero
Pillole di nutrizione e di prevenzione

L. Greco

2000/3 — pag. 163-166

RI Aggiornamento monografico
Accesso libero
Capire la nutrizione. Come si sbaglia e come si possono correggere gli errori

C. Galluzzo, M. Giovannini

2000/2 — pag. 85-89

Nutrition is, paradoxically, a major health problem in Italy as in other industrialized countries. Infant and child diet is usually unbalanced, improperly rich in saturated fats and proteins with a low fiber content. It is very difficult to face t...

RI ABC
Accesso libero
La febbre e il suo laboratorio

F. Panizon

1999/8 — pag. 512-514

RI Focus
Accesso libero
Sindrome da antifosfolipidi

A. Ravelli, A. Martini

1999/6 — pag. 362-370

RI ABC
Accesso libero
Integrazioni minerali e vitaminiche dopo il primo anno di vita

F. Panizon

1998/9 — pag. 600-603