Literature DB >> 11808885

Normal pituitary function in a Japanese patient with Barth syndrome.

Yuriko Katsushima, Ikuma Fujiwara, Osamu Sakamoto, Toshihiro Ohura, Shigeaki Miyabayashi, Akira Ohnuma, Seiji Yamaguchi, Kazuie Iinuma.   

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Year:  2002        PMID： 11808885     DOI： 10.1007/s00431-001-0869-5

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  6 in total

1.  Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.

Authors:  S B Bleyl; B R Mumford; V Thompson; J C Carey; T J Pysher; T K Chin; K Ward
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

2.  Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.

Authors:  A M Cantlay; K Shokrollahi; J T Allen; P W Lunt; R A Newbury-Ecob; C G Steward
Journal:  J Pediatr       Date:  1999-09       Impact factor: 4.406

3.  Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia.

Authors:  A Quade; S Zierz; D Klingmüller
Journal:  Clin Investig       Date:  1992-05

4.  An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

Authors:  P G Barth; H R Scholte; J A Berden; J M Van der Klei-Van Moorsel; I E Luyt-Houwen; E T Van 't Veer-Korthof; J J Van der Harten; M A Sobotka-Plojhar
Journal:  J Neurol Sci       Date:  1983-12       Impact factor: 3.181

5.  The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

Authors:  P D'Adamo; L Fassone; A Gedeon; E A Janssen; S Bione; P A Bolhuis; P G Barth; M Wilson; E Haan; K H Orstavik; M A Patton; A J Green; E Zammarchi; M A Donati; D Toniolo
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

6.  A novel X-linked gene, G4.5. is responsible for Barth syndrome.

Authors:  S Bione; P D'Adamo; E Maestrini; A K Gedeon; P A Bolhuis; D Toniolo
Journal:  Nat Genet       Date:  1996-04       Impact factor: 38.330
  6 in total
  1 in total

Review 1.  TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome.

Authors:  Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping
Journal:  Gene       Date:  2019-10-21       Impact factor: 3.688
  1 in total

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