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Literature DB >> 10720020

Acute ischemic stroke in a young woman with the thiamine-responsive megaloblastic anemia syndrome.

V Villa¹, A Rivellese, F Di Salle, C Iovine, V Poggi, B Capaldo.

Abstract

Entities: Chemical Disease Species

Mesh：

Substances：
Thiamine

Year: 2000 PMID： 10720020 DOI： 10.1210/jcem.85.3.6419

Source DB: PubMed Journal: J Clin Endocrinol Metab ISSN： 0021-972X Impact factor: 5.958

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Cited

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8 in total

1. Thiamine responsive megaloblastic anemia in three Indian children.

Authors: Vykunta Raju K N Gowda; Govindaraj M Shivananda; Naveen Sankhyan
Journal: Indian J Pediatr Date: 2011-02-22 Impact factor: 1.967

2. Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.

Authors: Prapaporn Jungtrakoon; Jun Shirakawa; Patinut Buranasupkajorn; Manoj K Gupta; Dario F De Jesus; Marcus G Pezzolesi; Aussara Panya; Timothy Hastings; Chutima Chanprasert; Christine Mendonca; Rohit N Kulkarni; Alessandro Doria
Journal: Diabetes Date: 2019-03-04 Impact factor: 9.461

3. Thiamine-responsive megaloblastic anemia syndrome.

Authors: Ali Bay; Mehmet Keskin; Samil Hizli; Hatice Uygun; Alper Dai; Fatma Gumruk
Journal: Int J Hematol Date: 2010-09-11 Impact factor: 2.490

4. Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update.

Authors: Anke K Bergmann; Inderneel Sahai; Jill F Falcone; Judy Fleming; Adam Bagg; Caterina Borgna-Pignati; Robin Casey; Luca Fabris; Elizabeth Hexner; Lulu Mathews; Maria Leticia Ribeiro; Klaas J Wierenga; Ellis J Neufeld
Journal: J Pediatr Date: 2009-07-29 Impact factor: 4.406

Acute ischemic stroke in a young woman with the thiamine-responsive megaloblastic anemia syndrome.

1. Thiamine responsive megaloblastic anemia in three Indian children.

2. Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.

3. Thiamine-responsive megaloblastic anemia syndrome.

4. Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update.

5. Thiamine responsive megaloblastic anemia syndrome.

6. Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?

7. Stroke as an Initial Manifestation of Thiamine-Responsive Megaloblastic Anemia.

8. Recurrent Stroke in a Child with TRMA Syndrome and SLC19A2 Gene Mutation.