Mixed Function Oxygenases

Non solo ginecomastia peripuberale… aromatase excess syndrome (AEXES)

M. Mauro, L. Baggio, P. Cavarzere

2018/1

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-...

Cifoscoliosi, ipotonia e iperlassità ligamentosa alla nascita: a quale sindrome pensare?

L. Matarazzo, C. Zanchi

2014/8

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...

La fenilchetonuria

2010/7 — pag. 461-462

...E se il Dotto Arterioso Pervio persiste nonostante la terapia con ibuprofene?

A. Secinaro, E. Antonielli d'Olux, P. Manzoni, D. Farina, M. L. Leonessa, G. Gomirato

2006/7

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

Gli anticonvulsivanti riducono l'efficacia della chemioterapia nella leucemia

G. Bartolozzi

2000/7