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J Coll

Showing results (91-100 of 344) with videos related to

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Human Mutation|January 29, 2000
Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definitionC Busquets, M J Coll, A Ribes
Journal of Inherited Metabolic Disease|October 8, 1998
Hunter disease in the Spanish population: molecular analysis in 31 familiesL Gort, A Chabás, M J Coll
Human Mutation|September 8, 1999
Identification of 12 novel mutations and two new polymorphisms in the arylsulfatase A gene: haplotype and genotype-phenotype correlation studies in Spanish metachromatic leukodystrophy patientsL Gort, M J Coll, A Chabás
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|December 1, 1978
[Study of blood thyroid hormones in 98 deaf children]J Coll, G Dutau, Hoff, et al.
The Journal of Rheumatology|August 1, 1995
Interleukin-2 receptor expression in salivary glands of patients with Sjögren's syndromeJ Coll, S Tomás, R Vilella, et al.
Revista Clinica Espanola|December 1, 1985
[Incidence of Sjögren's syndrome in systemic scleroderma]J Coll, J Ferrando, J Vivancos, et al.
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|May 1, 1981
[Study childhood blindness-deafness: importance of auditory evoked potentials]J Coll, S Calvet, Y Lacomme, et al.
The American Journal of Medicine|March 1, 1992
Prevalence of Sjögren's syndrome in a neurology inpatient populationD Escudero, A Olive, P Latorre, et al.
Medicina Clinica|October 12, 1991
[Benign intracranial hypertension following the suspension of corticotherapy in a female patient previously operated on for Cushing's disease]A Lucas, J Coll, I Salinas, et al.
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|May 1, 1977
[Statistics on case finding in deafness in children]J Coll, M Rolland, C Sere, et al.
Pageof 35

Showing results (91-100 of 344) with videos related to

Sort By:
Pageof 35
Human Mutation|January 29, 2000
Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definitionC Busquets, M J Coll, A Ribes
Journal of Inherited Metabolic Disease|October 8, 1998
Hunter disease in the Spanish population: molecular analysis in 31 familiesL Gort, A Chabás, M J Coll
Human Mutation|September 8, 1999
Identification of 12 novel mutations and two new polymorphisms in the arylsulfatase A gene: haplotype and genotype-phenotype correlation studies in Spanish metachromatic leukodystrophy patientsL Gort, M J Coll, A Chabás
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|December 1, 1978
[Study of blood thyroid hormones in 98 deaf children]J Coll, G Dutau, Hoff, et al.
The Journal of Rheumatology|August 1, 1995
Interleukin-2 receptor expression in salivary glands of patients with Sjögren's syndromeJ Coll, S Tomás, R Vilella, et al.
Revista Clinica Espanola|December 1, 1985
[Incidence of Sjögren's syndrome in systemic scleroderma]J Coll, J Ferrando, J Vivancos, et al.
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|May 1, 1981
[Study childhood blindness-deafness: importance of auditory evoked potentials]J Coll, S Calvet, Y Lacomme, et al.
The American Journal of Medicine|March 1, 1992
Prevalence of Sjögren's syndrome in a neurology inpatient populationD Escudero, A Olive, P Latorre, et al.
Medicina Clinica|October 12, 1991
[Benign intracranial hypertension following the suspension of corticotherapy in a female patient previously operated on for Cushing's disease]A Lucas, J Coll, I Salinas, et al.
Journal Francais D'Oto-Rhino-Laryngologie; Audiophonologie, Chirurgie Maxillo-Faciale|May 1, 1977
[Statistics on case finding in deafness in children]J Coll, M Rolland, C Sere, et al.
Pageof 35