Y E HSIA
Overview
Explore the profile of Y E HSIA including associated specialties, affiliations and a list of published articles.
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Articles
81
Citations
667
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Recent Articles
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SHIM W, Derieg M, Powell B, HSIA Y
J Pediatr Surg
. 2000 Jan;
34(12):1853-5.
PMID: 10626872
Both pigmentation and otic defects of Waardenburg Syndrome and Hirschsprung's disease have a common origin in neural crest cells and were described in 1951 and 1887, respectively. The clinical manifestations...
3.
Hunt J, Lee L, Donlon T, HSIA Y
Br J Haematol
. 1999 Mar;
104(2):284-7.
PMID: 10050709
The region of the crossover causing the Filipino type of alpha thalassaemia has been determined by examining similarity between the regions which had been indicated as involved in the crossover...
4.
Hayward A, Ambruso D, Battaglia F, Donlon T, Eddelman K, Giller R, et al.
Fetal Diagn Ther
. 1998 May;
13(1):8-14.
PMID: 9605609
A fetus homozygous for alpha-thalassemia-1 was given haploidentical paternal CD34 cells at 13, 19 and 24 weeks' gestation and supported through pregnancy by blood transfusion. The fetal hematocrit ranged between...
5.
Bogart M, Fujita N, Serles L, HSIA Y
Am J Med Genet
. 1995 Oct;
59(1):36-7.
PMID: 8849007
We report on the prenatal diagnosis of a baby with a de novo centromeric fission of chromosome 21. Both fission products were mitotically stable. Follow-up chromosome analysis after birth confirmed...
6.
Neumann H, Lips C, HSIA Y, Zbar B
Brain Pathol
. 1995 Apr;
5(2):181-93.
PMID: 7670659
After a decade of intensive clinical and molecular genetic efforts the von Hippel-Lindau (VHL) gene was cloned in 1993. The open reading frame encodes the putative protein of 284 amino...
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Whaley J, Naglich J, Gelbert L, HSIA Y, Lamiell J, Green J, et al.
Am J Hum Genet
. 1994 Dec;
55(6):1092-102.
PMID: 7977367
von Hippel-Lindau (VHL) disease is a hereditary tumor syndrome predisposing to multifocal bilateral renal cell carcinomas (RCCs), pheochromocytomas, and pancreatic tumors, as well as angiomas and hemangioblastomas of the CNS....
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Shohat M, Lachman R, Gruber H, HSIA Y, Golbus M, Witt D, et al.
Am J Med Genet
. 1994 Aug;
52(1):9-18.
PMID: 7977470
To further characterize the clinical, radiographic and chondro-osseous morphologic changes in the Desbuquois syndrome, 7 patients from three sibships are described. They all had prenatal onset severe rhizomelic and mesomelic...