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Literature DB >> 3294362

Diffuse leiomyomatosis in Alport syndrome.

P Cochat¹, P Guibaud, R Garcia Torres, B Roussel, V Guarner, F Larbre.

Abstract

Entities: Disease

Mesh：

Year: 1988 PMID： 3294362 DOI： 10.1016/s0022-3476(88)80280-4

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

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Cited

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14 in total

1. Alport syndrome: a genetic study of 31 families.

Authors: R M'Rad; M Sanak; G Deschenes; J Zhou; C Bonaiti-Pellie; L Holvoet-Vermaut; S Heuertz; M C Gubler; M Broyer; J P Grunfeld
Journal: Hum Genet Date: 1992-12 Impact factor: 4.132

2. A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

Authors: D F Barker; C J Pruchno; X Jiang; C L Atkin; E M Stone; J C Denison; P R Fain; M C Gregory
Journal: Am J Hum Genet Date: 1996-06 Impact factor: 11.025

Review 3. Epidemiological and genetic clues for molecular mechanisms involved in uterine leiomyoma development and growth.

Authors: Arno E Commandeur; Aaron K Styer; Jose M Teixeira
Journal: Hum Reprod Update Date: 2015-07-03 Impact factor: 15.610

4. Young-onset peri-anorectal leiomyomatosis: report of a case.

Authors: Masahide Toshima; Koh Miura; Kazuyuki Ishida; Takayuki Mizoi; Takeshi Naitoh; Hitoshi Ogawa; Shinobu Ohnuma; Hiroyuki Sasaki; Kazuhiro Watanabe; Sho Haneda; Tomohiko Sase; Taiki Kajiwara; Yoshifumi Matsuda; Chikashi Shibata; Iwao Sasaki
Journal: Surg Today Date: 2012-05-19 Impact factor: 2.549

5. Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23.

Authors: Alexander Hoischen; Christina Landwehr; Sarah Kabisch; Xiao-Qi Ding; Detlef Trost; Gerhard Stropahl; Marianne Wigger; Bernhard Radlwimmer; Ruthild G Weber; Dieter Haffner
Journal: Pediatr Nephrol Date: 2009-05-15 Impact factor: 3.714

6. Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.

Authors: Simone Rost; Elisa Bach; Cordula Neuner; Indrajit Nanda; Sandra Dysek; Reginald E Bittner; Alexander Keller; Oliver Bartsch; Robert Mlynski; Thomas Haaf; Clemens R Müller; Erdmute Kunstmann
Journal: Eur J Hum Genet Date: 2013-05-29 Impact factor: 4.246

Diffuse leiomyomatosis in Alport syndrome.

1. Alport syndrome: a genetic study of 31 families.

2. A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

Review 3. Epidemiological and genetic clues for molecular mechanisms involved in uterine leiomyoma development and growth.

4. Young-onset peri-anorectal leiomyomatosis: report of a case.

5. Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23.

6. Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.

7. Developmental distribution of collagen IV isoforms and relevance to ocular diseases.

8. Reduced dermatopontin expression is a molecular link between uterine leiomyomas and keloids.

9. The association of anorectal leiomyomatosis and diffuse oesophageal leiomyomatosis.

Review 10. The spectrum of benign esophageal lesions: imaging findings.