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Klinische Wochenschrift
|
September 17, 1979
[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)]
D Pongratz, G Hübner, T Deufel, et al.
The Journal of Biological Chemistry
|
February 21, 1997
Functional characterization of a distinct ryanodine receptor mutation in human malignant hyperthermia-susceptible muscle
M Richter, L Schleithoff, T Deufel, et al.
Neuromuscular Disorders : NMD
|
June 8, 2000
A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homology
R Stucka, A Abicht, I H Song, et al.
The Clinical Investigator
|
February 1, 1993
The clinical spectrum of Friedreich's ataxia in German families showing linkage to the FRDA locus on chromosome 9
W Müller-Felber, T Rossmanith, C Spes, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
November 14, 1997
Determination of total homocysteine in human plasma by isocratic high-performance liquid chromatography
A Feussner, B Rolinski, N Weiss, et al.
Human Genetics
|
September 1, 1996
Yeast artificial chromosome mapping of the cystinosis locus on chromosome 17p by fluorescence in situ hybridization
I Stec, U Peters, E Harms, et al.
The Biochemical Journal
|
December 15, 1983
Catecholamine-induced insulin resistance of glucose transport in isolated rat adipocytes
D M Kirsch, M Baumgarten, T Deufel, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1985
[Mechanism and genetic control of the autoimmune response directed against beta-pancreatic cells in insulin-dependent diabetes]
B Michelsen, S Baekkeskov, T Deufel, et al.
Clinical Genetics
|
January 10, 2003
PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype
D Bönsch, C Neumann, R Lang-Roth, et al.
Medical and Pediatric Oncology
|
March 4, 1999
Development of ifosfamide-induced nephrotoxicity: prospective follow-up in 75 patients
R Rossi, J Pleyer, P Schäfers, et al.
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of 8
Search research articles
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Showing results (21-30 of 71) with videos related to
Sort By:
Page
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Klinische Wochenschrift
|
September 17, 1979
[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)]
D Pongratz, G Hübner, T Deufel, et al.
The Journal of Biological Chemistry
|
February 21, 1997
Functional characterization of a distinct ryanodine receptor mutation in human malignant hyperthermia-susceptible muscle
M Richter, L Schleithoff, T Deufel, et al.
Neuromuscular Disorders : NMD
|
June 8, 2000
A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homology
R Stucka, A Abicht, I H Song, et al.
The Clinical Investigator
|
February 1, 1993
The clinical spectrum of Friedreich's ataxia in German families showing linkage to the FRDA locus on chromosome 9
W Müller-Felber, T Rossmanith, C Spes, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
November 14, 1997
Determination of total homocysteine in human plasma by isocratic high-performance liquid chromatography
A Feussner, B Rolinski, N Weiss, et al.
Human Genetics
|
September 1, 1996
Yeast artificial chromosome mapping of the cystinosis locus on chromosome 17p by fluorescence in situ hybridization
I Stec, U Peters, E Harms, et al.
The Biochemical Journal
|
December 15, 1983
Catecholamine-induced insulin resistance of glucose transport in isolated rat adipocytes
D M Kirsch, M Baumgarten, T Deufel, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1985
[Mechanism and genetic control of the autoimmune response directed against beta-pancreatic cells in insulin-dependent diabetes]
B Michelsen, S Baekkeskov, T Deufel, et al.
Clinical Genetics
|
January 10, 2003
PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype
D Bönsch, C Neumann, R Lang-Roth, et al.
Medical and Pediatric Oncology
|
March 4, 1999
Development of ifosfamide-induced nephrotoxicity: prospective follow-up in 75 patients
R Rossi, J Pleyer, P Schäfers, et al.
Page
of 8