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J Melki

Showing results (41-50 of 79) with videos related to

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Nature Genetics|July 1, 1997
Correlation between severity and SMN protein level in spinal muscular atrophyS Lefebvre, P Burlet, Q Liu, et al.
Annales De Chirurgie|January 1, 1989
[Splenectomy in chronic idiopathic thrombopenic purpura in adults. Apropos of 49 cases]J Melki, J P Dauce, A Kunlin, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Journal of the Association for Research in Otolaryngology : JARO|February 11, 2014
A mouse model validates the utility of electrocochleography in verifying endolymphatic hydropsSami J Melki, Yiping Li, Maroun T Semaan, et al.
Lancet (London, England)|July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophyL Bürglen, R Spiegel, J Ignatius, et al.
The Journal of Cardiovascular Surgery|December 1, 1995
Resection of the aorta for leiomyosarcoma of the inferior vena cavaP Soury, J Riviere, J Melki, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 22, 2011
Hearing preservation in Guinea pigs with long-standing endolymphatic hydropsSuhael R Momin, Sami J Melki, Joy O Obokhare, et al.
Journal of Medical Genetics|June 1, 1997
SMN gene analysis of the spinal form of Charcot-Marie-Tooth diseaseA Hanash, E Leguern, N Birouk, et al.
Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Developmental Biology|March 1, 1989
Nerve and muscle development in paralysé mutant miceB Blondet, M J Duxson, A J Harris, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
Nature Genetics|July 1, 1997
Correlation between severity and SMN protein level in spinal muscular atrophyS Lefebvre, P Burlet, Q Liu, et al.
Annales De Chirurgie|January 1, 1989
[Splenectomy in chronic idiopathic thrombopenic purpura in adults. Apropos of 49 cases]J Melki, J P Dauce, A Kunlin, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Journal of the Association for Research in Otolaryngology : JARO|February 11, 2014
A mouse model validates the utility of electrocochleography in verifying endolymphatic hydropsSami J Melki, Yiping Li, Maroun T Semaan, et al.
Lancet (London, England)|July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophyL Bürglen, R Spiegel, J Ignatius, et al.
The Journal of Cardiovascular Surgery|December 1, 1995
Resection of the aorta for leiomyosarcoma of the inferior vena cavaP Soury, J Riviere, J Melki, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 22, 2011
Hearing preservation in Guinea pigs with long-standing endolymphatic hydropsSuhael R Momin, Sami J Melki, Joy O Obokhare, et al.
Journal of Medical Genetics|June 1, 1997
SMN gene analysis of the spinal form of Charcot-Marie-Tooth diseaseA Hanash, E Leguern, N Birouk, et al.
Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Developmental Biology|March 1, 1989
Nerve and muscle development in paralysé mutant miceB Blondet, M J Duxson, A J Harris, et al.
Pageof 8