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Journal of Inherited Metabolic Disease
|
October 13, 1999
Transcobalamin II deficiency with methylmalonic aciduria in three sisters
H Bibi, Z Gelman-Kohan, E R Baumgartner, et al.
Zeitschrift Fur Gastroenterologie
|
November 1, 1976
[Complications and side effects in the fiber endoscopy of the upper gastrointestinal tract]
R Gassmann, R Baumgartner, M L Hefti, et al.
Laryngo- Rhino- Otologie
|
November 30, 2002
[Fluorescence staining of oral and laryngeal cancer after application of 5-aminolevulinic acid]
A Leunig, C S Betz, P Heinrich, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome
C Bannwart, B Wermuth, R Baumgartner, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1989
[Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H]
J Nothjunge, I Krägeloh-Mann, T M Suormala, et al.
Brain & Development
|
September 18, 2007
Recurrent attacks of status epilepticus as predominant symptom in 3-methylcrotonyl-CoA carboxylase deficiency
Eray Dirik, Uluç Yiş, Güven Paşaoğlu, et al.
Biochimica Et Biophysica Acta
|
April 28, 1973
Changes in the physicochemical characteristics of rabbit liver N-acetyltransferase during post-natal development
S N Cohen, R Baumgartner, M S Steinberg, et al.
Zeitschrift Fur Gastroenterologie
|
December 1, 1974
[Erosive gastritis, erosive duodenitis]
H Stocker, R Baumgartner, R Gassmann, et al.
Human Mutation
|
August 3, 2000
mut0 methylmalonic acidemia: eleven novel mutations of the methylmalonyl CoA mutase including a deletion-insertion mutation
A Fuchshuber, B Mucha, E R Baumgartner, et al.
Tierarztliche Praxis
|
August 1, 1993
[Anesthesia and immobilization in reptiles]
B J Schildger, R Baumgartner, W Häfeli, et al.
Page
of 77
Search research articles
Search
Showing results (301-310 of 770) with videos related to
Sort By:
Page
of 77
Journal of Inherited Metabolic Disease
|
October 13, 1999
Transcobalamin II deficiency with methylmalonic aciduria in three sisters
H Bibi, Z Gelman-Kohan, E R Baumgartner, et al.
Zeitschrift Fur Gastroenterologie
|
November 1, 1976
[Complications and side effects in the fiber endoscopy of the upper gastrointestinal tract]
R Gassmann, R Baumgartner, M L Hefti, et al.
Laryngo- Rhino- Otologie
|
November 30, 2002
[Fluorescence staining of oral and laryngeal cancer after application of 5-aminolevulinic acid]
A Leunig, C S Betz, P Heinrich, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome
C Bannwart, B Wermuth, R Baumgartner, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1989
[Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H]
J Nothjunge, I Krägeloh-Mann, T M Suormala, et al.
Brain & Development
|
September 18, 2007
Recurrent attacks of status epilepticus as predominant symptom in 3-methylcrotonyl-CoA carboxylase deficiency
Eray Dirik, Uluç Yiş, Güven Paşaoğlu, et al.
Biochimica Et Biophysica Acta
|
April 28, 1973
Changes in the physicochemical characteristics of rabbit liver N-acetyltransferase during post-natal development
S N Cohen, R Baumgartner, M S Steinberg, et al.
Zeitschrift Fur Gastroenterologie
|
December 1, 1974
[Erosive gastritis, erosive duodenitis]
H Stocker, R Baumgartner, R Gassmann, et al.
Human Mutation
|
August 3, 2000
mut0 methylmalonic acidemia: eleven novel mutations of the methylmalonyl CoA mutase including a deletion-insertion mutation
A Fuchshuber, B Mucha, E R Baumgartner, et al.
Tierarztliche Praxis
|
August 1, 1993
[Anesthesia and immobilization in reptiles]
B J Schildger, R Baumgartner, W Häfeli, et al.
Page
of 77