Search research articles
Contact Us
Filters
Showing results (31-40 of 71) with videos related to
Page
of 8
Sort By:
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1983
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle
J Müller-Höcker, D Pongratz, T Deufel, et al.
Neurology
|
February 16, 2006
Unexpected pathogenic mechanism of a novel mutation in the coding sequence of SPG4 (spastin)
J Schickel, C Beetz, C Frömmel, et al.
Human Mutation
|
January 1, 1994
Identification of a novel missense mutation (G314E) in exon 7 of the cystic fibrosis transmembrane conductance regulator gene identified in a CF patient with pancreatic sufficiency
A Golla, A Deufel, C Aulehla-Scholz, et al.
Archives of Neurology
|
October 28, 1997
Features, symptoms, and neurophysiological findings in stroke associated with hyperhomocysteinemia
S Evers, H G Koch, K H Grotemeyer, et al.
Clinical Chemistry and Laboratory Medicine
|
June 25, 1998
External quality assessment of molecular biology-based methods used in laboratories of clinical chemistry and human genetics
A Braun, T Deufel, W J Geilenkeuser, et al.
Dermatology (Basel, Switzerland)
|
June 6, 2008
Effect of regular sauna on epidermal barrier function and stratum corneum water-holding capacity in vivo in humans: a controlled study
D Kowatzki, C Macholdt, K Krull, et al.
Human Mutation
|
January 1, 1994
Three novel mutations (I506S, S466X, 1651A-->T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of southern German descent
A Deufel, T Deufel, A Golla, et al.
Endocrinology
|
March 1, 1997
Thyrotropin expression in hypophyseal pars tuberalis-specific cells is 3,5,3'-triiodothyronine, thyrotropin-releasing hormone, and pit-1 independent
J Bockmann, T M Böckers, C Winter, et al.
HNO
|
February 3, 2009
[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter]
D Bönsch, C-M Schmidt, P Scheer, et al.
Human Molecular Genetics
|
December 1, 1993
In frame deletion (delta F311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene
T Meitinger, A Golla, C Dörner, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1983
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle
J Müller-Höcker, D Pongratz, T Deufel, et al.
Neurology
|
February 16, 2006
Unexpected pathogenic mechanism of a novel mutation in the coding sequence of SPG4 (spastin)
J Schickel, C Beetz, C Frömmel, et al.
Human Mutation
|
January 1, 1994
Identification of a novel missense mutation (G314E) in exon 7 of the cystic fibrosis transmembrane conductance regulator gene identified in a CF patient with pancreatic sufficiency
A Golla, A Deufel, C Aulehla-Scholz, et al.
Archives of Neurology
|
October 28, 1997
Features, symptoms, and neurophysiological findings in stroke associated with hyperhomocysteinemia
S Evers, H G Koch, K H Grotemeyer, et al.
Clinical Chemistry and Laboratory Medicine
|
June 25, 1998
External quality assessment of molecular biology-based methods used in laboratories of clinical chemistry and human genetics
A Braun, T Deufel, W J Geilenkeuser, et al.
Dermatology (Basel, Switzerland)
|
June 6, 2008
Effect of regular sauna on epidermal barrier function and stratum corneum water-holding capacity in vivo in humans: a controlled study
D Kowatzki, C Macholdt, K Krull, et al.
Human Mutation
|
January 1, 1994
Three novel mutations (I506S, S466X, 1651A-->T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of southern German descent
A Deufel, T Deufel, A Golla, et al.
Endocrinology
|
March 1, 1997
Thyrotropin expression in hypophyseal pars tuberalis-specific cells is 3,5,3'-triiodothyronine, thyrotropin-releasing hormone, and pit-1 independent
J Bockmann, T M Böckers, C Winter, et al.
HNO
|
February 3, 2009
[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter]
D Bönsch, C-M Schmidt, P Scheer, et al.
Human Molecular Genetics
|
December 1, 1993
In frame deletion (delta F311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene
T Meitinger, A Golla, C Dörner, et al.
Page
of 8