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V Muller

Showing results (31-40 of 45) with videos related to

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The Journal of Biological Chemistry|November 1, 1996
Feline mucopolysaccharidosis type VI. Characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseG Yogalingam, T Litjens, J Bielicki, et al.
The American Journal of Physiology|June 1, 1997
Gestational resistance to the pulmonary vasoconstrictor effect of the TxA2 mimetic U-46619: possible mechanismG Losonczy, G Brown, I Mucha, et al.
The Medical Journal of Australia|March 20, 1982
Enzymatic diagnosis of the mucopolysaccharidoses: experience of 96 cases diagnosed in a five-year periodJ J Hopwood, V Muller, J R Harrison, et al.
Transplantation Proceedings|August 10, 2010
Spontaneous pneumomediastinum after kidney transplantation: case reportA Kis, Z Sutto, L Tamasi, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|October 21, 2016
Ectopic pregnancy following in vitro fertilization: meta-analysis and single-center experience during 6 yearsV Muller, M Makhmadalieva, I Kogan, et al.
The Japanese Journal of Human Genetics|June 1, 1997
Mucopolysaccharidosis IVA: a novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an Afghanistan girl with classical Morquio diseaseS Fukuda, N Yamada, S Tomatsu, et al.
The Medical Journal of Australia|February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight yearsW F Carey, J J Hopwood, A Poulos, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patientsR Gatti, P DiNatale, G R Villani, et al.
Medical Teacher|April 6, 2017
Interprofessional collaborative reasoning by residents and nurses in internal medicine: Evidence from a simulation studyK S Blondon, F Maître, V Muller-Juge, et al.
Human Mutation|April 1, 1998
Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotypeN Yamada, S Fukuda, S Tomatsu, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
The Journal of Biological Chemistry|November 1, 1996
Feline mucopolysaccharidosis type VI. Characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseG Yogalingam, T Litjens, J Bielicki, et al.
The American Journal of Physiology|June 1, 1997
Gestational resistance to the pulmonary vasoconstrictor effect of the TxA2 mimetic U-46619: possible mechanismG Losonczy, G Brown, I Mucha, et al.
The Medical Journal of Australia|March 20, 1982
Enzymatic diagnosis of the mucopolysaccharidoses: experience of 96 cases diagnosed in a five-year periodJ J Hopwood, V Muller, J R Harrison, et al.
Transplantation Proceedings|August 10, 2010
Spontaneous pneumomediastinum after kidney transplantation: case reportA Kis, Z Sutto, L Tamasi, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|October 21, 2016
Ectopic pregnancy following in vitro fertilization: meta-analysis and single-center experience during 6 yearsV Muller, M Makhmadalieva, I Kogan, et al.
The Japanese Journal of Human Genetics|June 1, 1997
Mucopolysaccharidosis IVA: a novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an Afghanistan girl with classical Morquio diseaseS Fukuda, N Yamada, S Tomatsu, et al.
The Medical Journal of Australia|February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight yearsW F Carey, J J Hopwood, A Poulos, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patientsR Gatti, P DiNatale, G R Villani, et al.
Medical Teacher|April 6, 2017
Interprofessional collaborative reasoning by residents and nurses in internal medicine: Evidence from a simulation studyK S Blondon, F Maître, V Muller-Juge, et al.
Human Mutation|April 1, 1998
Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotypeN Yamada, S Fukuda, S Tomatsu, et al.
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