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Michael Ludwig

Showing results (121-130 of 239) with videos related to

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Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadiasMarkus Draaken, Judith Proske, Charlotte Schramm, et al.
Hormone Research in Paediatrics|October 27, 2017
Targeted Resequencing of Putative Growth-Related Genes Using Whole Exome Sequencing in Patients with Severe Primary IGF-I DeficiencyGreta Grosse, Alina Hilger, Michael Ludwig, et al.
European Journal of Pediatrics|September 30, 2011
Liddle syndrome in a Serbian family and literature review of underlying mutationsRadovan Bogdanović, Vladimir Kuburović, Nataša Stajić, et al.
Human Genetics|May 17, 2005
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalizationMichael Ludwig, Jolanta Doroszewicz, Hannsjörg W Seyberth, et al.
Pediatric Nephrology (Berlin, Germany)|January 21, 2011
Clinical and laboratory features of Macedonian children with OCRL mutationsVelibor Tasic, Vladimir J Lozanovski, Petar Korneti, et al.
Pediatric Nephrology (Berlin, Germany)|October 21, 2005
R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasiaArend Bökenkamp, Miranda deJong, Joanna A E van Wijk, et al.
European Journal of Pediatrics|October 17, 2008
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literatureHeiko Reutter, Arend Bökenkamp, Anne-Karolin Ebert, et al.
Neuroscience Letters|July 19, 2008
Deletion of both ICAM-1 and C3 enhances severity of experimental autoimmune encephalomyelitis compared to C3-deficient miceSherry S Smith, Michael Ludwig, Jillian E Wohler, et al.
Journal of Pediatric Genetics|September 15, 2016
Novel OCRL mutations in patients with Dent-2 diseaseDetlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, et al.
Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Pageof 24

Showing results (121-130 of 239) with videos related to

Sort By:
Pageof 24
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadiasMarkus Draaken, Judith Proske, Charlotte Schramm, et al.
Hormone Research in Paediatrics|October 27, 2017
Targeted Resequencing of Putative Growth-Related Genes Using Whole Exome Sequencing in Patients with Severe Primary IGF-I DeficiencyGreta Grosse, Alina Hilger, Michael Ludwig, et al.
European Journal of Pediatrics|September 30, 2011
Liddle syndrome in a Serbian family and literature review of underlying mutationsRadovan Bogdanović, Vladimir Kuburović, Nataša Stajić, et al.
Human Genetics|May 17, 2005
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalizationMichael Ludwig, Jolanta Doroszewicz, Hannsjörg W Seyberth, et al.
Pediatric Nephrology (Berlin, Germany)|January 21, 2011
Clinical and laboratory features of Macedonian children with OCRL mutationsVelibor Tasic, Vladimir J Lozanovski, Petar Korneti, et al.
Pediatric Nephrology (Berlin, Germany)|October 21, 2005
R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasiaArend Bökenkamp, Miranda deJong, Joanna A E van Wijk, et al.
European Journal of Pediatrics|October 17, 2008
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literatureHeiko Reutter, Arend Bökenkamp, Anne-Karolin Ebert, et al.
Neuroscience Letters|July 19, 2008
Deletion of both ICAM-1 and C3 enhances severity of experimental autoimmune encephalomyelitis compared to C3-deficient miceSherry S Smith, Michael Ludwig, Jillian E Wohler, et al.
Journal of Pediatric Genetics|September 15, 2016
Novel OCRL mutations in patients with Dent-2 diseaseDetlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, et al.
Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Pageof 24