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R D Cohn

Showing results (11-20 of 25) with videos related to

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Obstetrics and Gynecology|March 1, 1984
Atenolol in human plasma and breast milkW B White, J W Andreoli, S H Wong, et al.
Human Molecular Genetics|March 23, 2018
Increased polyamines as protective disease modifiers in congenital muscular dystrophyD U Kemaladewi, J S Benjamin, E Hyatt, et al.
Clinical Genetics|March 28, 2015
The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicineS C Bowdin, R Z Hayeems, N Monfared, et al.
Neuromuscular Disorders : NMD|April 30, 1999
Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardationT Voit, R D Cohn, J Sperner, et al.
The Journal of Clinical Investigation|February 13, 2001
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complexR D Cohn, M Durbeej, S A Moore, et al.
American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndromeA von Moers, F K van Landeghem, R D Cohn, et al.
Journal of the Neurological Sciences|June 17, 1999
Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscleR D Cohn, U Mayer, G Saher, et al.
Lancet (London, England)|June 1, 2000
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathyW M Franz, M Müller, O J Müller, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Obstetrics and Gynecology|March 1, 1984
Atenolol in human plasma and breast milkW B White, J W Andreoli, S H Wong, et al.
Human Molecular Genetics|March 23, 2018
Increased polyamines as protective disease modifiers in congenital muscular dystrophyD U Kemaladewi, J S Benjamin, E Hyatt, et al.
Clinical Genetics|March 28, 2015
The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicineS C Bowdin, R Z Hayeems, N Monfared, et al.
Neuromuscular Disorders : NMD|April 30, 1999
Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardationT Voit, R D Cohn, J Sperner, et al.
The Journal of Clinical Investigation|February 13, 2001
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complexR D Cohn, M Durbeej, S A Moore, et al.
American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndromeA von Moers, F K van Landeghem, R D Cohn, et al.
Journal of the Neurological Sciences|June 17, 1999
Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscleR D Cohn, U Mayer, G Saher, et al.
Lancet (London, England)|June 1, 2000
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathyW M Franz, M Müller, O J Müller, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Pageof 3