Hemeproteins

Artrite e osteomielite in età pediatrica: un esordio insidioso di drepanocitosi?

Di Marcoberardino F, Camelli V, Filice E, Stera G, De Agostini M, Mengozzi E, Guerra L, Ghizzi C

2026/2 — pag. 43-44 — DOI

This report describes the case of a 13-month-old boy presenting with fever, pain and functional limitation of the right elbow. Initial findings suggested septic arthritis and led to empirical antibiotic treatment. Subsequent diagnostic evaluation, wh...

Dolore e colore: tre neretti addolorati

2025/5 — pag. 292-295 — DOI

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...

Il bambino con anemia severa: proposta di gestione diagnostico-terapeutica

Muratore E, Ruggi A, Abram N, Zanaroli A, Pierantoni L, Lanari M, Zama D.

2023/3 — pag. 159-168 — DOI

Anaemia is a common issue in the paediatric age group and it is not uncommon to encounter severe cases of anaemia in the Paediatric Emergency Unit. The correct identification of patients requiring urgent care is of central importance to provide timel...

Ittero, pallore e urine scure: e se fosse un’anemia emolitica autoimmune?

Tessitore A, Putoto E, Romano F, Verzegnassi F, Barbi E, Cozzi G, Parodi E.

2022/7 — pag. 451-455 — DOI

The haemolytic crisis is a sudden reduction in the half-life of red blood cells. Consequently, it leads to massive destruction of red blood cells (haemolysis), which is more significant than the compensatory capacity of the bone marrow and results in...

Un vaccino falcemico

Sambugaro D

2021/6 — pag. 394-394 — DOI

A case of a sickle cell crisis initially diagnosed as post vaccination arthritis is described. The author stresses the high specificity of acute dactylitis with respect to the diagnosis of sickle cell anaemia....

Una grave anemizzazione

M. Cognigni

2020/9 — pag. 599 — DOI

Anemia falciforme e sindrome toracica acuta

G. Graziani, J. Gencarelli, C. Lama, S. Brocchi, L. Biserna, C. Radice, F. Marchetti

2020/6 — pag. 392-394

Anemia falciforme e sindrome toracica acuta

G. Graziani, J. Gencarelli, C. Lama, S. Brocchi, L. Biserna, C. Radice, F. Marchetti

2020/6 — pag. 126-129 — DOI

La malattia drepanocitica in Pronto Soccorso

M. Casale, S. Perrotta, G. Russo, L. Sainati, R. Colombatti, G.L. Forni

2019/10 — pag. 639-644

Sickle cell disease is the most common genetic disorder observed at emergency units worldwide with more and more children being diagnosed with severe acute events. Emergency caregivers need to be aware of potentially life-threatening complications ...

Intossicazione da monossido di carbonio

F. Quarantiello, F. Gallicola, L. Timpone

2019/2 — pag. 83-90

Carbon monoxide (CO) poisoning is one of the main causes of poisoning and death due to intoxication in nowadays society because of the characteristics of this gas, which make it unidentifiable in the environment, and of the many possible sources of...

Non solo ginecomastia peripuberale… aromatase excess syndrome (AEXES)

M. Mauro, L. Baggio, P. Cavarzere

2018/1

La gestione condivisa ospedale-territorio del bambino con malattia drepanocitica

P. Samperi, R. Colombatti, E. Cannata, L. Sainati, G. Russo

2017/10 — pag. 629-635

Sickle cell disease is a hereditary autosomal disease of haemoglobin characterized by chronic haemolytic anaemia, vaso-occlusive painful crisis, organ damage and increased susceptibility to infections. In recent years, the number of patients with s...

Un blu che non ritorna: cosa c’entra l’emoglobina Cincinnati?

M. Magnani, V. Silecchia, L. Marchetto, C. Vallongo, C. Gentilomo

2017/10

L’anemia che fa male

A. Bonadies, G. Rispoli

2017/7 — pag. 465-466

L’anemia che fa male

A. Bonadies, G. Rispoli

2017/7

La ginecomastia: cosa deve sapere il pediatra

M.C. Pellegrin, G. Patti, E. Faleschini, G. Tornese, A. Ventura

2016/6 — pag. 357-363

Gynecomastia is the glandular proliferation of male breast tissue, involving up to 65% of men in their lifetime. It is often a benign condition, but it can be the sign of a serious endocrine disease and the source of significant physical and psycho...

Insufficienza surrenalica: rara ma non troppo

G. Patti, G. Tornese, M.C. Pellegrin, K. Vecchiato, E. Faleschini, A. Ventura

2016/1 — pag. 21-26

Adrenal insufficiency is a rare condition in childhood. Clinical characteristics of adrenal insufficiency in children may be non-specific. Therefore, the diagnosis may be suspected late. If unrecognized, adrenal insufficiency may present with life-...

Una famiglia con il collo che ciondola

I. Giuseppin, M. Ranieri, A. Camolese, A. Tonetto, P.G. Flora

2015/9 — pag. 598-600

Anemia sideropenica nel III millennio“Nuovi” parametri di monitoraggio della risposta terapeutica

E. Parodi, M.L. Aurucci, B. Stella, G. Russo, U. Ramenghi

2015/8 — pag. 515-519

Iron deficiency and iron deficiency anaemia (IDA) secondary to inadequate dietary iron intake are still in the third millennium the most common nutritional disorder and the most common haematological diseases of infancy and childhood. The article d...

Una tumefazione del clitoride

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

2014/2 — pag. 113-115

La Codeina nell’adenotonsillectomia: nuove evidenze di rischio per un vecchio farmaco

V. Murgia

2013/5 — pag. 328-330

La Codeina nell’adenotonsillectomia: nuove evidenze di rischio per un vecchio farmaco

V. Murgia

2013/5

Rachitismo vitamina D-resistente: dalla clinica alla genetica, “andata e ritorno”

G.I. Baroncelli, B. Toschi, L. Cinquanta, P. Manfredi, A. Rossodivita, A. Michelucci, F. Baldinotti, S. Bertelloni

2013/2 — pag. 89-99

The term “vitamin D-resistant rickets” was used to describe a clinical condition which was indistinguishable from the common rickets except that the signs occurred in spite of adequate vitamin D treatment. Recent studies showed that vitamin D-resis...

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...

Dalle curve di crescita alla diagnosi di sindrome adrenogenitale

D. Cimino, V. Giacchi

2012/7 — pag. 463-464

Non-classical congenital adrenal hyperplasia (NC CAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms (premature pubarche, accelerated growth, advanced bone age, penile enlargement, and hypertrophy of...

Dalle curve di crescita alla diagnosi di sindrome adrenogenitale

D. Cimino, V. Giacchi

2012/7

Non-classical congenital adrenal hyperplasia (NC CAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms (premature pubarche, accelerated growth, advanced bone age, penile enlargement, and hypertrophy of...

Lo studio funzionale della corteccia cerebrale mediante la topografia ottica nel neonato

A. Clarici, S. Bembich, L. Travan, C. Oretti, C. Vecchiet, M. Bava, P. Brovedani, E. Neri, S. Massaccesi, T. Farroni, S. Demarini

2010/1 — pag. 41-46

Optical topography is a non-invasive functional brain imaging technique, which uses light in the near infra-red spectrum and allows to detect hemodynamic changes in the cerebral cortex. Specifically, it measures relative changes in oxygenated, de-o...

Una trasfusione va sempre bene per i ricoverati in terapia intensiva pediatrica?

G. Bartolozzi

2007/8

Anemie facili e difficili

U. Ramenghi

2007/1 — pag. 27-31

Most forms of anemias in childhood are easy to diagnose. A decreased mean corpuscolar volume (MCV) is due to reduced hemoglobin synthesis and suggests iron deficiency or thalassemia. Anemia with a normal MCV is mainly due to hemolysis or hemorrhage...

L'anemia falciforme

M. Lazzerini, M. Rabusin

2006/4 — pag. 223-234

Sickle cell disease (SCD) is one of the most prevalent haemoglobinopathies in the world, being related to areas where malaria is or was endemic. In Italy the majority of patients still live in Sicily, where the overall HbS gene frequency is 2%. Domes...

ß-talassemia (Parte prima)

G. Bartolozzi

2006/1

Sindrome adreno-genitale congenita da deficit di 21-idrossilasi

A. Balsamo, A. Cicognani

2005/5 — pag. 293-301

Congenital adrenal hyperplasia (CAH) refers to a group of inherited disorders of adrenal steroidogenesis. More than 90% of CAH is due to 21-hydroxylase deficiency (21-OH-D), found in 1:10.000 to 1:15.000 live births as classical form and detected i...

Eritromicina per bocca e rischio di morte improvvisa

G. Bartolozzi

2004/9

Precisazioni sull’emocromoFluoroprofilassiAncora sul costo dei latti!

2004/7 — pag. 423

Leggere l’emocromo

I. Bruno

2004/2 — pag. 113-115

Quandoque bonus dormitat HomerusIl giusto e l’onestoCeliachia dell’adultoInfezioni e interventi chirurgici?Non partecipo a SPES: chi sono, perché non partecipo, cosa faccio invece

2002/10 — pag. 642-644

Vomito e diarrea come sintoma di presentazione di un' intossicazione da ossido di carbonio

G. Nocerino

2001/7

Gli anticonvulsivanti riducono l'efficacia della chemioterapia nella leucemia

G. Bartolozzi

2000/7

Le β-talassemie

1999/8