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The Quarterly Journal of Medicine
|
April 1, 1987
Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews
A Zimran, B Rudensky, M R Kramer, et al.
British Journal of Haematology
|
December 12, 2001
High prevalence of low serum vitamin B12 in a multi-ethnic Israeli population
Y Gielchinsky, D Elstein, R Green, et al.
Lancet (London, England)
|
October 14, 1995
Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype
A Abrahamov, D Elstein, V Gross-Tsur, et al.
Lancet (London, England)
|
June 10, 1995
Replacement therapy with imiglucerase for type 1 Gaucher's disease
A Zimran, D Elstein, E Levy-Lahad, et al.
Blood Cells, Molecules & Diseases
|
July 10, 2003
The 1226G (N370S) Gaucher mutation among patients with Legg-Calve-Perthes disease
G Kenet, S Hayek, M Mor, et al.
The Journal of Pediatrics
|
April 1, 1995
Outcome of partial splenectomy for type I Gaucher disease
A Zimran, D Elstein, R Schiffmann, et al.
Human Genetics
|
June 16, 1999
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease
E K Lau, N Tayebi, L J Ingraham, et al.
Pediatric Research
|
January 1, 1996
Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease
E Sidransky, M Fartasch, R E Lee, et al.
Lancet (London, England)
|
May 9, 2000
Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis
T Cox, R Lachmann, C Hollak, et al.
Archives of Internal Medicine
|
October 12, 2000
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, H C Andersson, P Kaplan, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 135) with videos related to
Sort By:
Page
of 14
The Quarterly Journal of Medicine
|
April 1, 1987
Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews
A Zimran, B Rudensky, M R Kramer, et al.
British Journal of Haematology
|
December 12, 2001
High prevalence of low serum vitamin B12 in a multi-ethnic Israeli population
Y Gielchinsky, D Elstein, R Green, et al.
Lancet (London, England)
|
October 14, 1995
Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype
A Abrahamov, D Elstein, V Gross-Tsur, et al.
Lancet (London, England)
|
June 10, 1995
Replacement therapy with imiglucerase for type 1 Gaucher's disease
A Zimran, D Elstein, E Levy-Lahad, et al.
Blood Cells, Molecules & Diseases
|
July 10, 2003
The 1226G (N370S) Gaucher mutation among patients with Legg-Calve-Perthes disease
G Kenet, S Hayek, M Mor, et al.
The Journal of Pediatrics
|
April 1, 1995
Outcome of partial splenectomy for type I Gaucher disease
A Zimran, D Elstein, R Schiffmann, et al.
Human Genetics
|
June 16, 1999
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease
E K Lau, N Tayebi, L J Ingraham, et al.
Pediatric Research
|
January 1, 1996
Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease
E Sidransky, M Fartasch, R E Lee, et al.
Lancet (London, England)
|
May 9, 2000
Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis
T Cox, R Lachmann, C Hollak, et al.
Archives of Internal Medicine
|
October 12, 2000
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, H C Andersson, P Kaplan, et al.
Page
of 14