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M Doss

Showing results (91-100 of 180) with videos related to

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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 kidneyM Doss, R von Tiepermann, K H Pflüger
Clinical Genetics|September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiencyM 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 syndromeM Frank, M Doss, D G de Carvalho
Current Medicinal Chemistry. Anti-Cancer Agents|August 17, 2005
Programmable DNA binding oligomers for control of transcriptionPeter B Dervan, Raymond M Doss, Michael A Marques
Experimental and Clinical Endocrinology|August 1, 1985
Clinical and experimental investigations of vasopressin secretion in acute porphyriasU 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 manifestationM 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 stateM Doss, J Schneider, R Von Tiepermann, et al.
Pageof 18

Showing results (91-100 of 180) with videos related to

Sort By:
Pageof 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 kidneyM Doss, R von Tiepermann, K H Pflüger
Clinical Genetics|September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiencyM 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 syndromeM Frank, M Doss, D G de Carvalho
Current Medicinal Chemistry. Anti-Cancer Agents|August 17, 2005
Programmable DNA binding oligomers for control of transcriptionPeter B Dervan, Raymond M Doss, Michael A Marques
Experimental and Clinical Endocrinology|August 1, 1985
Clinical and experimental investigations of vasopressin secretion in acute porphyriasU 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 manifestationM 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 stateM Doss, J Schneider, R Von Tiepermann, et al.
Pageof 18