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Australasian Radiology
|
August 2, 2003
A prospective trial of short-fractionation radiotherapy for the palliation of liver metastases
S Bydder, N A Spry, D R H Christie, et al.
The Journal of Experimental Medicine
|
October 1, 1996
Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease
J H Leusen, A de Klein, P M Hilarius, et al.
Orvosi Hetilap
|
February 16, 1997
[Chronic granulomatous disease (CGD): dysfunction of the neutrophil granulocyte NADPH-oxidase enzyme system]
K Német, G Fekete, D Schuler, et al.
Blood
|
March 25, 2000
A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia
E Ristoff, C Augustson, J Geissler, et al.
Hemoglobin
|
May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl
H M van den Berg, M C Bruin, D Batelaan, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 1, 1981
T lymphocyte characteristics in bone marrow-transplanted patients. I. Changes in biochemical properties that correlate with the immunologic reconstitution
R J van de Griend, A Astaldi, J M Vossen, et al.
Blood
|
March 1, 1996
Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
D Roos, M de Boer, F Kuribayashi, et al.
Australian and New Zealand Journal of Medicine
|
May 26, 1999
Osteolymphoma (primary bone lymphoma): an Australian review of 70 cases. Australasian Radiation Oncology Lymphoma Group (AROLG)
D R Christie, M B Barton, G Bryant, et al.
Blood
|
May 16, 1998
Human eosinophils express, relative to other circulating leukocytes, large amounts of secretory 14-kD phospholipase A2
M Blom, A T Tool, P C Wever, et al.
Blood
|
May 1, 1981
Effect of ascorbate on abnormal neutrophil, platelet and lymphocytic function in a patient with the Chediak-Higashi syndrome
R S Weening, E P Schoorel, D Roos, et al.
Page
of 43
Search research articles
Search
Showing results (391-400 of 422) with videos related to
Sort By:
Page
of 43
Australasian Radiology
|
August 2, 2003
A prospective trial of short-fractionation radiotherapy for the palliation of liver metastases
S Bydder, N A Spry, D R H Christie, et al.
The Journal of Experimental Medicine
|
October 1, 1996
Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease
J H Leusen, A de Klein, P M Hilarius, et al.
Orvosi Hetilap
|
February 16, 1997
[Chronic granulomatous disease (CGD): dysfunction of the neutrophil granulocyte NADPH-oxidase enzyme system]
K Német, G Fekete, D Schuler, et al.
Blood
|
March 25, 2000
A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia
E Ristoff, C Augustson, J Geissler, et al.
Hemoglobin
|
May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl
H M van den Berg, M C Bruin, D Batelaan, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 1, 1981
T lymphocyte characteristics in bone marrow-transplanted patients. I. Changes in biochemical properties that correlate with the immunologic reconstitution
R J van de Griend, A Astaldi, J M Vossen, et al.
Blood
|
March 1, 1996
Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
D Roos, M de Boer, F Kuribayashi, et al.
Australian and New Zealand Journal of Medicine
|
May 26, 1999
Osteolymphoma (primary bone lymphoma): an Australian review of 70 cases. Australasian Radiation Oncology Lymphoma Group (AROLG)
D R Christie, M B Barton, G Bryant, et al.
Blood
|
May 16, 1998
Human eosinophils express, relative to other circulating leukocytes, large amounts of secretory 14-kD phospholipase A2
M Blom, A T Tool, P C Wever, et al.
Blood
|
May 1, 1981
Effect of ascorbate on abnormal neutrophil, platelet and lymphocytic function in a patient with the Chediak-Higashi syndrome
R S Weening, E P Schoorel, D Roos, et al.
Page
of 43