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Search Results - Martari, M
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The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes
by
Stratakis, CA
,
Tichomirowa, MA
,
Boikos, S
,
Azevedo, MF
,
Lodish, M
,
Martari, M
,
Verma, S
,
Daly, AF
,
Raygada, M
,
Keil, MF
,
Papademetriou, J
,
Drori-Herishanu, L
,
Horvath, A
,
Tsang, KM
,
Nesterova, M
,
Franklin, S
,
Vanbellinghen, J-F
,
Bours, V
,
Salvatori, R
,
Beckers, A
Published in
Clinical genetics
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Longevity in Untreated Congenital Growth Hormone Deficiency Due to a Homozygous Mutation in the GHRH Receptor Gene
by
Aguiar-Oliveira, Manuel H
,
Oliveira, Francielle T
,
Pereira, Rossana M. C
,
Oliveira, Carla R. P
,
Blackford, Amanda
,
Valenca, Eugenia H. O
,
Santos, Elenilde G
,
Gois-Junior, Miburge B
,
Meneguz-Moreno, Rafael A
,
Araujo, Vanessa P
,
Oliveira-Neto, Luis A
,
Almeida, Roque P
,
Santos, Mário A
,
Farias, Natalia T
,
Silveira, Debora C. R
,
Cabral, Gabriel W
,
Calazans, Flavia R
,
Seabra, Juliane D
,
Lopes, Tiago F
,
Rodrigues, Endrigo O
,
Porto, Livia A
,
Oliveira, Igor P
,
Melo, Enaldo V
,
Martari, Marco
,
Salvatori, Roberto
Published in
The journal of clinical endocrinology and metabolism
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Clinical Genetics
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The Journal Of Clinical Endocrinology And Metabolism
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The Journal Of Clinical Endocrinology And Metabolism/Journal Of Clinical Endocrinology & Metabolism
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Science Citation Index Expanded (Web Of Science)
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