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1
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome

Thatiana Evilen da Silva Mirian Yumie Nishi; Elaine Maria Frade Costa; Regina Matsunaga Martin; Filomena Marino Carvalho; Berenice Bilharinho Mendonça; Sorahia Domenice

Pediatric nephrology Berlin v. 26, n. 8, p. 1311-1315, 2011

Berlin 2011

Localização: FM - Fac. Medicina    (BCSEP 073 2011 )(Acessar)

2
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome

Thatiana Evilen da Silva Mirian Yumie Nishi; Elaine Maria Frade Costa; Regina Matsunaga Martin; Filomena Marino Carvalho; Berenice Bilharinho Mendonça; Sorahia Domenice

Pediatric nephrology Berlin v. 26, n. 8, p. 1311-1315, 2011

Berlin 2011

Localização: FM - Fac. Medicina    (BCSEP 073 2011 )(Acessar)

3
Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors
Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors

Maria Candida B Villares Fragoso Ana Claudia Latronico; Filomena Marino Carvalho; Maria Cláudia Nogueira Zerbini; Jose Antonio Miguel Marcondes; Leila M B Araujo; Valeria S Lando; Eliana T Frazzatto; Berenice Bilharinho de Mendonça; Sandra Mara F Villares

The Journal of Clinical Endocrinology & Metabolism v. 83, n. 6, p. 2074-2078, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

4
Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors
Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal leydig cell tumors

Maria Candida B Villares Fragoso Ana Claudia Latronico; Filomena Marino Carvalho; Maria Cláudia Nogueira Zerbini; Jose Antonio Miguel Marcondes; Leila M B Araujo; Valeria S Lando; Eliana T Frazzatto; Berenice Bilharinho de Mendonça; Sandra Mara F Villares

The Journal of Clinical Endocrinology & Metabolism v. 83, n. 6, p. 2074-2078, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

5
Persistent Poor Metabolic Profile in Postmenopausal Women With Ovarian Hyperandrogenism After Testosterone Level Normalization
Persistent Poor Metabolic Profile in Postmenopausal Women With Ovarian Hyperandrogenism After Testosterone Level Normalization
Material Type:
Artigo 		Adicionar ao Meu Espaço

Persistent Poor Metabolic Profile in Postmenopausal Women With Ovarian Hyperandrogenism After Testosterone Level Normalization

Thais Rocha Raiane P Crespo; Viviane V. R Yance; Sylvia A Hayashida; Edmund Chada Baracat; Filomena Marino Carvalho; Sorahia Domenice; Berenice Bilharinho de Mendonça; Larissa G Gomes

Journal of the endocrine society v. 3, n. 5, p. 1087-1096, 2019

Washington 2019

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Mendonça, B
  2. Carvalho, F
  3. Domenice, S
  4. Costa, E
  5. Latronico, A

Neste Assunto:

  1. Medicina
  2. Mutação Genética
  3. Evolução Clínica
  4. Proteinúria
  5. Nefropatias (Genética)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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