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Search Results - TORPIANO, John
Search Results - TORPIANO, John
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A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
by
Whittaker, Danielle E
,
Oleari, Roberto
,
Gregory, Louise C
,
Le Quesne-Stabej, Polona
,
Williams, Hywel J
,
Torpiano, John G
,
Formosa, Nancy
,
Cachia, Mario J
,
Field, Daniel
,
Lettieri, Antonella
,
Ocaka, Louise A
,
Paganoni, Alyssa Jj
,
Rajabali, Sakina H
,
Riegman, Kimberley Lh
,
De Martini, Lisa B
,
Chaya, Taro
,
Robinson, Iain Caf
,
Furukawa, Takahisa
,
Cariboni, Anna
,
Basson, M Albert
,
Dattani, Mehul T
Published in
The Journal of clinical investigation
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Congenital brachymetatarsia and Turner syndrome
by
Formosa, Nancy
,
Buttigieg, Mark
,
Torpiano, John
Published in
Archives of disease in childhood
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Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency
by
Turton, James P. G
,
Reynaud, Rachel
,
Mehta, Ameeta
,
Torpiano, John
,
Saveanu, Alexandru
,
Woods, Kathryn S
,
Tiulpakov, Anatoly
,
Zdravkovic, Vera
,
Hamilton, Jill
,
Attard-Montalto, Simon
,
Parascandalo, Ray
,
Vella, Cecil
,
Clayton, Peter E
,
Shalet, Stephen
,
Barton, John
,
Brue, Thierry
,
Dattani, Mehul T
Published in
The journal of clinical endocrinology and metabolism
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Incidence and modes of presentation of childhood type 1 diabetes mellitus in Malta between 2006 and 2010
by
Formosa, Nancy
,
Calleja, Neville
,
Torpiano, John
Published in
Pediatric diabetes
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Cushing syndrome in a child due to pro-opiomelanocortin (POMC) secretion from a yolk sac tumor
by
Gevers, Evelien F
,
Meredith, Suzanne
,
Shah, Pratik
,
Torpiano, John
,
Peters, Catherine
,
Sebire, Neil J
,
Slater, Olga
,
White, Anne
,
Dattani, Mehul T
Published in
European journal of endocrinology
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Incidence and modes of presentation of childhood type 1 diabetes mellitus in Malta between 2006 and 2010: Incidence of T1DM in Maltese children
by
Formosa, Nancy
,
Calleja, Neville
,
Torpiano, John
Published in
Pediatric diabetes
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Acanthosis Nigricans and Insulin Sensitivity in Patients with Achondroplasia and Hypochodroplasia due to FGFR3 Mutations
by
Alatzoglou, Kyriaki S
,
Hindmarsh, Peter C
,
Brain, Caroline
,
Torpiano, John
,
Dattani, Mehul T
Published in
The journal of clinical endocrinology and metabolism
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Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency
by
TURTON, James P. G
,
REYNAUD, Rachel
,
PARASCANDALO, Ray
,
VELLA, Cecil
,
CLAYTON, Peter E
,
SHALET, Stephen
,
BARTON, John
,
BRUE, Thierry
,
DATTANI, Mehul T
,
MEHTA, Ameeta
,
TORPIANO, John
,
SAVEANU, Alexandru
,
WOODS, Kathryn S
,
TIULPAKOV, Anatoly
,
ZDRAVKOVIC, Vera
,
HAMILTON, Jill
,
ATTARD-MONTALTO, Simon
Published in
The journal of clinical endocrinology and metabolism
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Intrathoracic schwannoma with Horner syndrome
by
Torpiano, Paul
,
Borg, Elaine
,
Cassar, Paul John
,
Manche’, Alexander
Published in
BMJ case reports
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Intrathoracic schwannoma with Horner syndrome
by
Torpiano, Paul
,
Borg, Elaine
,
Cassar, Paul John
,
Manche’, Alexander
Published in
BMJ Case Reports
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