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Dorothea Wand

Showing results (1-10 of 16) with videos related to

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Pathologie (Heidelberg, Germany)|January 15, 2026
[Unexpected death of a two-year-old child: How electron microscopy helped to identify the potential cause]Thomas Menter, Dorothea Wand, Maya Caroline André
Pathologie (Heidelberg, Germany)|May 6, 2026
Thomas Menter, Dorothea Wand, Maya Caroline André
International Journal of Legal Medicine|May 2, 2024
Zygotic-splitting after in vitro fertilization and prenatal parenthood testing after suspected embryo mix-up - a case reportIris Schulz, Janine Schulte, Dorothea Wand Dipl-Med
Case Reports in Neurology|January 14, 2021
Fragile-X-Associated Tremor/Ataxia Syndrome or Alcohol-Induced Cerebellar Degeneration? A Case ReportGiulia Grigioni, Christian Saleh, Phillip Jaszczuk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 17, 2013
Low-level hyperinsulinism with hypoglycemic spells in an infant with mosaic Turner syndrome and mild Kabuki-like phenotype: a case report and review of the literatureVera Pietzner, Johannes F W Weigel, Dorothea Wand, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 30, 2021
Gelsolin-Amyloidosis - An Exceptional Cause of BlepharochalasisFaady Yahya, Eva Kesenheimer, Bernhard F Decard, et al.
Muscle & Nerve|January 17, 2012
SOX10 mutation with peripheral amyelination and developmental disturbance of axonsKathleen Parthey, Malte Kornhuber, Christian Kunze, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findingsAnja Hagen, Arndt Bigl, Dorothea Wand, et al.
Human Mutation|August 19, 2006
Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutationsWiktor Borozdin, Ana M Bravo Ferrer Acosta, Michael J Bamshad, et al.
American Journal of Medical Genetics. Part A|May 11, 2005
Association of migraine-like headaches with Schimke immuno-osseous dysplasiaSara Sebnem Kilic, Osman Donmez, Emily A Sloan, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Pathologie (Heidelberg, Germany)|January 15, 2026
[Unexpected death of a two-year-old child: How electron microscopy helped to identify the potential cause]Thomas Menter, Dorothea Wand, Maya Caroline André
Pathologie (Heidelberg, Germany)|May 6, 2026
Thomas Menter, Dorothea Wand, Maya Caroline André
International Journal of Legal Medicine|May 2, 2024
Zygotic-splitting after in vitro fertilization and prenatal parenthood testing after suspected embryo mix-up - a case reportIris Schulz, Janine Schulte, Dorothea Wand Dipl-Med
Case Reports in Neurology|January 14, 2021
Fragile-X-Associated Tremor/Ataxia Syndrome or Alcohol-Induced Cerebellar Degeneration? A Case ReportGiulia Grigioni, Christian Saleh, Phillip Jaszczuk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 17, 2013
Low-level hyperinsulinism with hypoglycemic spells in an infant with mosaic Turner syndrome and mild Kabuki-like phenotype: a case report and review of the literatureVera Pietzner, Johannes F W Weigel, Dorothea Wand, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 30, 2021
Gelsolin-Amyloidosis - An Exceptional Cause of BlepharochalasisFaady Yahya, Eva Kesenheimer, Bernhard F Decard, et al.
Muscle & Nerve|January 17, 2012
SOX10 mutation with peripheral amyelination and developmental disturbance of axonsKathleen Parthey, Malte Kornhuber, Christian Kunze, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findingsAnja Hagen, Arndt Bigl, Dorothea Wand, et al.
Human Mutation|August 19, 2006
Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutationsWiktor Borozdin, Ana M Bravo Ferrer Acosta, Michael J Bamshad, et al.
American Journal of Medical Genetics. Part A|May 11, 2005
Association of migraine-like headaches with Schimke immuno-osseous dysplasiaSara Sebnem Kilic, Osman Donmez, Emily A Sloan, et al.
Pageof 2