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Literature DB >> 14149008

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

Abstract

Entities: Disease Gene

Keywords: CHILD; DISEASES IN TWINS; GENETICS, HUMAN; GONADOTROPINS; NEOPLASMS, EMBRYONAL AND MIXED; NEPHROTIC SYNDROME; PATHOLOGY; SERTOLI CELL TUMOR; SEX DETERMINATION; THECA CELL TUMOR; TURNER'S SYNDROME

Mesh：

Substances：
Gonadotropins

Year: 1964 PMID： 14149008 DOI： 10.1016/s0022-3476(64)80622-3

Source DB: PubMed Journal: J Pediatr ISSN： 0022-3476 Impact factor: 4.406

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Cited

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46 in total

Review 1. Frasier and Denys-Drash syndromes: different disorders or part of a spectrum?

Authors: A Koziell; R Grundy
Journal: Arch Dis Child Date: 1999-10 Impact factor: 3.791

2. [AN XX/XY-HERMAPHRODITE WITH AN "INTRATUBULAR OVUM" AND A GONADOBLASTOMA (GONOCYTOMA 3)].

Authors: C OVERZIER
Journal: Klin Wochenschr Date: 1964-11-01

Review 3. Educational paper: the podocytopathies.

Authors: Anja K Büscher; Stefanie Weber
Journal: Eur J Pediatr Date: 2012-01-13 Impact factor: 3.183

4. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.

Authors: Spyridon Megremis; Andromachi Mitsioni; Irene Fylaktou; Sofia Kitsiou Tzeli; Filadelfia Komianou; Constantinos J Stefanidis; Emmanuel Kanavakis; Joanne Traeger-Synodinos
Journal: Eur J Pediatr Date: 2011-04-16 Impact factor: 3.183

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

Review 1. Frasier and Denys-Drash syndromes: different disorders or part of a spectrum?

2. [AN XX/XY-HERMAPHRODITE WITH AN "INTRATUBULAR OVUM" AND A GONADOBLASTOMA (GONOCYTOMA 3)].

Review 3. Educational paper: the podocytopathies.

4. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.

5. Prepubertal gonadoblastoma in a 46,XY female patient with features of Turner syndrome.

6. Three sisters with gonadoblastoma.

Review 7. Genetic causes of proteinuria and nephrotic syndrome: impact on podocyte pathobiology.

8. Molecular analysis of chromosome region 11p13 in patients with Drash syndrome.

Review 9. Membranous nephropathy associated with ovarian tumour in a young girl: recovery after removal.

10. Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.