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P Huppke

Showing results (1-10 of 23) with videos related to

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Neuropediatrics|November 19, 2010
A practical guide to pediatric multiple sclerosisP Huppke, J Gärtner
Human Mutation|March 10, 2001
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regionsF Laccone, P Huppke, F Hanefeld, et al.
Clinical Dysmorphology|January 29, 2000
Two brothers with Hennekam syndrome and cerebral abnormalitiesP Huppke, H J Christen, B Sattler, et al.
Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, et al.
Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.
Neuropediatrics|June 21, 2002
Influence of mutation type and location on phenotype in 123 patients with Rett syndromeP Huppke, M Held, F Hanefeld, et al.
Der Nervenarzt|October 18, 2017
[Multiple sclerosis in childhood and adolescence : Complex, chronic and differentiated]A Blaschek, P Huppke, T Kümpfel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.
Annals of Hematology|November 1, 1994
Mutations in the R-type pyruvate kinase gene and altered enzyme kinetic properties in patients with hemolytic anemia due to pyruvate kinase deficiencyM Lakomek, P Huppke, B Neubauer, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Neuropediatrics|November 19, 2010
A practical guide to pediatric multiple sclerosisP Huppke, J Gärtner
Human Mutation|March 10, 2001
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regionsF Laccone, P Huppke, F Hanefeld, et al.
Clinical Dysmorphology|January 29, 2000
Two brothers with Hennekam syndrome and cerebral abnormalitiesP Huppke, H J Christen, B Sattler, et al.
Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, et al.
Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.
Neuropediatrics|June 21, 2002
Influence of mutation type and location on phenotype in 123 patients with Rett syndromeP Huppke, M Held, F Hanefeld, et al.
Der Nervenarzt|October 18, 2017
[Multiple sclerosis in childhood and adolescence : Complex, chronic and differentiated]A Blaschek, P Huppke, T Kümpfel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.
Annals of Hematology|November 1, 1994
Mutations in the R-type pyruvate kinase gene and altered enzyme kinetic properties in patients with hemolytic anemia due to pyruvate kinase deficiencyM Lakomek, P Huppke, B Neubauer, et al.
Pageof 3