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The New England Journal of Medicine
|
February 15, 1990
Neurologic crises in hereditary tyrosinemia
G Mitchell, J Larochelle, M Lambert, et al.
Annals of Neurology
|
July 1, 1993
Myoblast transfer in Duchenne muscular dystrophy
G Karpati, D Ajdukovic, D Arnold, et al.
Neurogenetics
|
March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7
C F Rochette, L C Surh, P N Ray, et al.
The Journal of Pediatrics
|
November 1, 1992
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients
J F Lemay, M A Lambert, G A Mitchell, et al.
Brain : a Journal of Neurology
|
June 9, 2006
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21
M Tétreault, A Duquette, I Thiffault, et al.
American Journal of Medical Genetics. Part A
|
October 26, 2022
Teaching perspectives on the communication of difficult news of genetic conditions to medical students
Ashley M Vanasse, Tracey Weiler, Elizabeth A Roth, et al.
Lancet (London, England)
|
September 18, 2001
Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research Group
J P Collet, M Vanasse, P Marois, et al.
Brain : a Journal of Neurology
|
May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34
I Thiffault, M F Rioux, M Tetreault, et al.
Neurology
|
May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians
K Roddier, T Thomas, G Marleau, et al.
Annals of Neurology
|
May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion
L Montermini, A Richter, K Morgan, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
The New England Journal of Medicine
|
February 15, 1990
Neurologic crises in hereditary tyrosinemia
G Mitchell, J Larochelle, M Lambert, et al.
Annals of Neurology
|
July 1, 1993
Myoblast transfer in Duchenne muscular dystrophy
G Karpati, D Ajdukovic, D Arnold, et al.
Neurogenetics
|
March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7
C F Rochette, L C Surh, P N Ray, et al.
The Journal of Pediatrics
|
November 1, 1992
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients
J F Lemay, M A Lambert, G A Mitchell, et al.
Brain : a Journal of Neurology
|
June 9, 2006
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21
M Tétreault, A Duquette, I Thiffault, et al.
American Journal of Medical Genetics. Part A
|
October 26, 2022
Teaching perspectives on the communication of difficult news of genetic conditions to medical students
Ashley M Vanasse, Tracey Weiler, Elizabeth A Roth, et al.
Lancet (London, England)
|
September 18, 2001
Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research Group
J P Collet, M Vanasse, P Marois, et al.
Brain : a Journal of Neurology
|
May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34
I Thiffault, M F Rioux, M Tetreault, et al.
Neurology
|
May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians
K Roddier, T Thomas, G Marleau, et al.
Annals of Neurology
|
May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion
L Montermini, A Richter, K Morgan, et al.
Page
of 5