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Clinical and Experimental Immunology
|
October 27, 2001
X-linked lymphoproliferative disease: three atypical cases
K Nistala, K C Gilmour, T Cranston, et al.
International Journal of Sports Medicine
|
April 14, 2006
Pulmonary O2 uptake on-kinetics in endurance- and sprint-trained master athletes
N J A Berger, J Rittweger, A Kwiet, et al.
Antimicrobial Agents and Chemotherapy
|
December 14, 2016
Fungal CYP51 Inhibitors VT-1161 and VT-1129 Exhibit Strong <i>In Vitro</i> Activity against Candida glabrata and C. krusei Isolates Clinically Resistant to Azole and Echinocandin Antifungal Compounds
W A Schell, A M Jones, E P Garvey, et al.
Journal of Medical Genetics
|
September 1, 1994
Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis
T Lester, M de Alwis, P A Clark, et al.
Postgraduate Medical Journal
|
May 1, 1990
Spontaneous haemarthrosis following thrombolytic therapy for myocardial infarction
K G Oldroyd, R S Hornung, A M Jones, et al.
Transplantation Proceedings
|
February 11, 2014
Temsirolimus as base immunosuppressant for a recipient with metastatic renal cancer: adequate immunosuppression and oncological control--case report
S J Chueh, B R Sankari, R Gonzales-Chambers, et al.
Human Genetics
|
May 1, 1997
B-cell-negative severe combined immunodeficiency associated with a common gamma chain mutation
A M Jones, P A Clark, F Katz, et al.
The British Journal of Dermatology
|
April 14, 2020
Dermatological adverse events associated with use of oral mechanistic target of rapamycin inhibitors in a cohort of individuals with tuberous sclerosis complex
D J Pithadia, A M Treichel, A M Jones, et al.
Annals of Human Genetics
|
April 1, 1995
Complement component C6 and C7 haplotypes associated with deficiencies of C6
B A Fernie, A Orren, R Würzner, et al.
Human Molecular Genetics
|
January 1, 1994
Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis
L A Bradley, A K Sweatman, R C Lovering, et al.
Page
of 28
Search research articles
Search
Showing results (221-230 of 273) with videos related to
Sort By:
Page
of 28
Clinical and Experimental Immunology
|
October 27, 2001
X-linked lymphoproliferative disease: three atypical cases
K Nistala, K C Gilmour, T Cranston, et al.
International Journal of Sports Medicine
|
April 14, 2006
Pulmonary O2 uptake on-kinetics in endurance- and sprint-trained master athletes
N J A Berger, J Rittweger, A Kwiet, et al.
Antimicrobial Agents and Chemotherapy
|
December 14, 2016
Fungal CYP51 Inhibitors VT-1161 and VT-1129 Exhibit Strong <i>In Vitro</i> Activity against Candida glabrata and C. krusei Isolates Clinically Resistant to Azole and Echinocandin Antifungal Compounds
W A Schell, A M Jones, E P Garvey, et al.
Journal of Medical Genetics
|
September 1, 1994
Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis
T Lester, M de Alwis, P A Clark, et al.
Postgraduate Medical Journal
|
May 1, 1990
Spontaneous haemarthrosis following thrombolytic therapy for myocardial infarction
K G Oldroyd, R S Hornung, A M Jones, et al.
Transplantation Proceedings
|
February 11, 2014
Temsirolimus as base immunosuppressant for a recipient with metastatic renal cancer: adequate immunosuppression and oncological control--case report
S J Chueh, B R Sankari, R Gonzales-Chambers, et al.
Human Genetics
|
May 1, 1997
B-cell-negative severe combined immunodeficiency associated with a common gamma chain mutation
A M Jones, P A Clark, F Katz, et al.
The British Journal of Dermatology
|
April 14, 2020
Dermatological adverse events associated with use of oral mechanistic target of rapamycin inhibitors in a cohort of individuals with tuberous sclerosis complex
D J Pithadia, A M Treichel, A M Jones, et al.
Annals of Human Genetics
|
April 1, 1995
Complement component C6 and C7 haplotypes associated with deficiencies of C6
B A Fernie, A Orren, R Würzner, et al.
Human Molecular Genetics
|
January 1, 1994
Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis
L A Bradley, A K Sweatman, R C Lovering, et al.
Page
of 28