Niemann-Pick disease: Sixteen-year follow-up of allogeneic bone marrow transplantation in a type B variant-Reference-Cited by-同舟云学术

Niemann-Pick disease: Sixteen-year follow-up of allogeneic bone marrow transplantation in a type B variant

Published:2003-12 Issue:8 Volume:26 Page:775-785
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Victor S.¹,Coulter J. B. S.¹²,Besley G. T. N.³,Ellis I.¹,Desnick R. J.⁴,Schuchman E. H.⁴,Vellodi A.⁵

Affiliation:

1. Royal Liverpool Children's NHS Trust; Liverpool

2. Royal Liverpool Children's NHS Trust; Eaton Road Liverpool L12 2AP UK

3. ; Willink Biochemical Genetics Unit; Royal Manchester Children's Hospital; Manchester UK

4. ; Department ofHuman Genetics; Mount Sinai School of Medicine of New York University; NewYork USA

5. ; Great Ormond Street Hospital for Children NHS Trust; London UK

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000009950.81514.c8/fullpdf

Reference28 articles.

1. Bone marrow transplantation for Niemann Pick type IA disease;Bayever;J Inherit Metab Dis,1992

2. Enzyme activities and phospholipid storage patterns in brain and spleen samples from Niemann-Pick disease variants: a comparison of neuropathic and non-neuropathic forms;Besley;Jlnherit Metab Dis,1986

3. Retinal involvement with reticuloendotheliosis ofunclassified type;Cogan;Arch Ophthalmol,1964

4. Macular halo syndrome: variant of Niemann Pick disease;Cogan;Arch Ophthalmol,1983

5. Niemann-Pick disease (variation in the sphingomyelinase deficient group). Neurovisceral phenotype (A) with an abnormally protracted clinical course and vari-able expression of neurological symptomatology in three siblings;Elleder;Eur JPediatr,1983

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