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Eckhard Korsch

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

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Pediatrics|August 4, 2017
Re: Chang's Score Is Only Helpful Within the First 4 to 5 Days of LifeEckhard Korsch
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 26, 2020
["Crazy bitch!"-Experienced aggression and violence in the daily clinical routine of pediatricians]Antje Dresen, Susan Lee, Holger Pfaff, et al.
Hormone Research in Paediatrics|July 12, 2014
MKRN3 mutations in familial central precocious pubertyFelix Schreiner, Bettina Gohlke, Michaela Hamm, et al.
European Journal of Pediatrics|September 7, 2018
Inconsistencies in the management of neonates born to mothers with "thyroid diseases"Patricia C Weissenfels, Joachim Woelfle, Eckhard Korsch, et al.
Clinical Endocrinology|November 24, 2006
Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) geneNicole Pfarr, Eckhard Korsch, Stefan Kaspers, et al.
JIMD Reports|November 20, 2019
A mutation in mannose-phosphate-dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathyWalinka van Tol, Angel Ashikov, Eckhard Korsch, et al.
European Journal of Medical Genetics|March 23, 2011
Mosaic tetrasomy 14pterq13.1: longitudinal studyGesa Schwanitz, Eckhard Korsch, Ursula Kremens-Korsch, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14qThomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, et al.
European Journal of Pediatrics|March 31, 2016
Skin conductance in neonates suffering from abstinence syndrome and unexposed newbornsNicola Elisabeth Schubach, Katrin Mehler, Bernhard Roth, et al.
European Journal of Human Genetics : EJHG|March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermiaEva Morava, Renate Zeevaert, Eckhard Korsch, et al.
Pageof 2

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

Sort By:
Pageof 2
Pediatrics|August 4, 2017
Re: Chang's Score Is Only Helpful Within the First 4 to 5 Days of LifeEckhard Korsch
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 26, 2020
["Crazy bitch!"-Experienced aggression and violence in the daily clinical routine of pediatricians]Antje Dresen, Susan Lee, Holger Pfaff, et al.
Hormone Research in Paediatrics|July 12, 2014
MKRN3 mutations in familial central precocious pubertyFelix Schreiner, Bettina Gohlke, Michaela Hamm, et al.
European Journal of Pediatrics|September 7, 2018
Inconsistencies in the management of neonates born to mothers with "thyroid diseases"Patricia C Weissenfels, Joachim Woelfle, Eckhard Korsch, et al.
Clinical Endocrinology|November 24, 2006
Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) geneNicole Pfarr, Eckhard Korsch, Stefan Kaspers, et al.
JIMD Reports|November 20, 2019
A mutation in mannose-phosphate-dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathyWalinka van Tol, Angel Ashikov, Eckhard Korsch, et al.
European Journal of Medical Genetics|March 23, 2011
Mosaic tetrasomy 14pterq13.1: longitudinal studyGesa Schwanitz, Eckhard Korsch, Ursula Kremens-Korsch, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14qThomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, et al.
European Journal of Pediatrics|March 31, 2016
Skin conductance in neonates suffering from abstinence syndrome and unexposed newbornsNicola Elisabeth Schubach, Katrin Mehler, Bernhard Roth, et al.
European Journal of Human Genetics : EJHG|March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermiaEva Morava, Renate Zeevaert, Eckhard Korsch, et al.
Pageof 2