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Andrology
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August 28, 2016
Nicotinamide phosphoribosyltransferase production in human spermatozoa is influenced by maturation stage
S Riammer, A Garten, M Schaab, et al.
The Australian and New Zealand Journal of Psychiatry
|
September 1, 1994
Single photon emission computed tomography (SPECT) measures of brain function in schizophrenia
E Gordon, R J Barry, J Anderson, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I (CDG I)
M Jackson, P Clayton, S Grunewald, et al.
The British Journal of Dermatology
|
April 26, 2006
A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene
W Heinritz, S Grunewald, S Strenge, et al.
The British Journal of Dermatology
|
May 21, 2008
CD30+ anaplastic lymphoma kinase-positive anaplastic large cell lymphoma with an unusual translocation t(11;22)
M Schlaak, R Renner, R Treudler, et al.
European Journal of Nuclear Medicine
|
December 6, 2000
Reliability of DMSA for the diagnosis of renal parenchymal abnormality in children
J C Craig, L Irwig, M Ford, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2009
Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review
E J Footitt, A Karimova, M Burch, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
August 27, 2005
Vaccinations with T-helper type 1 directing adjuvants have different suppressive effects on the development of allergen-induced T-helper type 2 responses
C M Trujillo-Vargas, K D Mayer, T Bickert, et al.
The Journal of Clinical Investigation
|
January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
T Imbach, B Schenk, E Schollen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2008
Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations
B Pérez-Dueñas, A García-Cazorla, M Pineda, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 82) with videos related to
Sort By:
Page
of 9
Andrology
|
August 28, 2016
Nicotinamide phosphoribosyltransferase production in human spermatozoa is influenced by maturation stage
S Riammer, A Garten, M Schaab, et al.
The Australian and New Zealand Journal of Psychiatry
|
September 1, 1994
Single photon emission computed tomography (SPECT) measures of brain function in schizophrenia
E Gordon, R J Barry, J Anderson, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I (CDG I)
M Jackson, P Clayton, S Grunewald, et al.
The British Journal of Dermatology
|
April 26, 2006
A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene
W Heinritz, S Grunewald, S Strenge, et al.
The British Journal of Dermatology
|
May 21, 2008
CD30+ anaplastic lymphoma kinase-positive anaplastic large cell lymphoma with an unusual translocation t(11;22)
M Schlaak, R Renner, R Treudler, et al.
European Journal of Nuclear Medicine
|
December 6, 2000
Reliability of DMSA for the diagnosis of renal parenchymal abnormality in children
J C Craig, L Irwig, M Ford, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2009
Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review
E J Footitt, A Karimova, M Burch, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
August 27, 2005
Vaccinations with T-helper type 1 directing adjuvants have different suppressive effects on the development of allergen-induced T-helper type 2 responses
C M Trujillo-Vargas, K D Mayer, T Bickert, et al.
The Journal of Clinical Investigation
|
January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
T Imbach, B Schenk, E Schollen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2008
Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations
B Pérez-Dueñas, A García-Cazorla, M Pineda, et al.
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of 9