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Herz
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February 4, 2012
[Mitral valve surgery in patients with extensively calcified mitral annulus: long-term echocardiographic and clinical follow-up]
K Steuer, N Papadopoulos, A Moritz, et al.
Herz
|
November 19, 2011
[Long-term echocardiographic and clinical follow-up after mitral valve surgery in patients with extensive calcified mitral annulus]
K Steuer, N Papadopoulos, A Moritz, et al.
Journal of Neurology
|
January 1, 1981
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney
M Doss, R von Tiepermann, K H Pflüger
Clinical Genetics
|
September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiency
M Doss, H G Benkmann, H W Goedde
Journal of Neurology
|
May 18, 1978
[Diagnosis of acute intermittent porphyria. Results of neurological, biochemical and genetic studies]
K F Leonhardt, R v Tiepermann, M Doss
Hepato-Gastroenterology
|
February 1, 1990
Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in the Dubin-Johnson syndrome
M Frank, M Doss, D G de Carvalho
Current Medicinal Chemistry. Anti-Cancer Agents
|
August 17, 2005
Programmable DNA binding oligomers for control of transcription
Peter B Dervan, Raymond M Doss, Michael A Marques
Experimental and Clinical Endocrinology
|
August 1, 1985
Clinical and experimental investigations of vasopressin secretion in acute porphyrias
U Desaga, K F Leonhardt, H Frahm, et al.
Klinische Wochenschrift
|
October 15, 1979
New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation
M Doss, R von Tiepermann, J Schneider, et al.
Clinical Biochemistry
|
February 1, 1982
New type of acute porphyria with porphobilinogen synthase (delta-aminolevulinic acid dehydratase) defect in the homozygous state
M Doss, J Schneider, R Von Tiepermann, et al.
Page
of 18
Search research articles
Search
Showing results (91-100 of 180) with videos related to
Sort By:
Page
of 18
Herz
|
February 4, 2012
[Mitral valve surgery in patients with extensively calcified mitral annulus: long-term echocardiographic and clinical follow-up]
K Steuer, N Papadopoulos, A Moritz, et al.
Herz
|
November 19, 2011
[Long-term echocardiographic and clinical follow-up after mitral valve surgery in patients with extensive calcified mitral annulus]
K Steuer, N Papadopoulos, A Moritz, et al.
Journal of Neurology
|
January 1, 1981
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney
M Doss, R von Tiepermann, K H Pflüger
Clinical Genetics
|
September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiency
M Doss, H G Benkmann, H W Goedde
Journal of Neurology
|
May 18, 1978
[Diagnosis of acute intermittent porphyria. Results of neurological, biochemical and genetic studies]
K F Leonhardt, R v Tiepermann, M Doss
Hepato-Gastroenterology
|
February 1, 1990
Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in the Dubin-Johnson syndrome
M Frank, M Doss, D G de Carvalho
Current Medicinal Chemistry. Anti-Cancer Agents
|
August 17, 2005
Programmable DNA binding oligomers for control of transcription
Peter B Dervan, Raymond M Doss, Michael A Marques
Experimental and Clinical Endocrinology
|
August 1, 1985
Clinical and experimental investigations of vasopressin secretion in acute porphyrias
U Desaga, K F Leonhardt, H Frahm, et al.
Klinische Wochenschrift
|
October 15, 1979
New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation
M Doss, R von Tiepermann, J Schneider, et al.
Clinical Biochemistry
|
February 1, 1982
New type of acute porphyria with porphobilinogen synthase (delta-aminolevulinic acid dehydratase) defect in the homozygous state
M Doss, J Schneider, R Von Tiepermann, et al.
Page
of 18