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B Melegh

Showing results (51-60 of 99) with videos related to

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Biology of the Neonate|June 12, 1999
Labeled trimethyllysine load depletes unlabeled carnitine in premature infants without evidence of incorporationB Melegh, G Tóth, K Adamovich, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|March 5, 2009
Adenovirus gastroenteritis in Hungary, 2003-2006K Bányai, P Kisfali, A Bogdán, et al.
Orvosi Hetilap|June 3, 1998
[Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations]J Molnár, A Kis, B Melegh, et al.
Journal of Inherited Metabolic Disease|October 13, 1999
Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathyB Melegh, L Seress, T Bedekovics, et al.
Archives of Virology|December 4, 2003
Sequence heterogeneity among human picobirnaviruses detected in a gastroenteritis outbreakK Bányai, F Jakab, G Reuter, et al.
Acta Neurologica Scandinavica|February 7, 2004
Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosisZ Szolnoki, F Somogyvári, A Kondacs, et al.
American Journal of Medical Genetics|November 24, 1999
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian populationP Gyürüs, J Molnár, B Melegh, et al.
Human Mutation|June 30, 2000
Distribution of Q188R and N314D mutations in the Hungarian galactosemic populationA Horváth, P Gyurus, A Kis, et al.
Orvosi Hetilap|October 17, 2001
[Kennedy disease in a patient with progressive speech disorder]J Kárteszi, E Morava, M Czakó, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Partial craniosynostosis in a patient with deletion 22q11J Karteszi, W Kress, M Szasz, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Biology of the Neonate|June 12, 1999
Labeled trimethyllysine load depletes unlabeled carnitine in premature infants without evidence of incorporationB Melegh, G Tóth, K Adamovich, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|March 5, 2009
Adenovirus gastroenteritis in Hungary, 2003-2006K Bányai, P Kisfali, A Bogdán, et al.
Orvosi Hetilap|June 3, 1998
[Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations]J Molnár, A Kis, B Melegh, et al.
Journal of Inherited Metabolic Disease|October 13, 1999
Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathyB Melegh, L Seress, T Bedekovics, et al.
Archives of Virology|December 4, 2003
Sequence heterogeneity among human picobirnaviruses detected in a gastroenteritis outbreakK Bányai, F Jakab, G Reuter, et al.
Acta Neurologica Scandinavica|February 7, 2004
Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosisZ Szolnoki, F Somogyvári, A Kondacs, et al.
American Journal of Medical Genetics|November 24, 1999
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian populationP Gyürüs, J Molnár, B Melegh, et al.
Human Mutation|June 30, 2000
Distribution of Q188R and N314D mutations in the Hungarian galactosemic populationA Horváth, P Gyurus, A Kis, et al.
Orvosi Hetilap|October 17, 2001
[Kennedy disease in a patient with progressive speech disorder]J Kárteszi, E Morava, M Czakó, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Partial craniosynostosis in a patient with deletion 22q11J Karteszi, W Kress, M Szasz, et al.
Pageof 10