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Catharina Whybra

Showing results (1-10 of 26) with videos related to

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Zeitschrift Fur Geburtshilfe Und Neonatologie|June 6, 2020
[Results of the hypothermia registry of the University Hospital Dresden from 2010-2017. Application of hypothermia therapy in newborns in Germany]Jonas Scherer, Catharina Whybra-Trümpler, Eva Mildenberger
Acta Paediatrica (Oslo, Norway : 1992)|March 19, 2020
Non-immune hydrops fetalis was rare in Sweden during 1997-2015, but cases were associated with complications and poor prognosisCatharina Whybra, Karin Källén, Stefan R Hansson, et al.
European Cytokine Network|March 14, 2007
An association study of inflammatory cytokine gene polymorphisms in Fabry diseaseRachael Safyan, Catharina Whybra, Michael Beck, et al.
Klinische Padiatrie|July 19, 2017
Weaning Premature Infants from Nasal Continuous Positive Airway Pressure - Current Practice and Scientific EvidenceAndré Kidszun, Christine Arnold, Julia Winter, et al.
Nephron. Clinical Practice|July 20, 2010
Paraoxonase (PON1) gene polymorphisms in Fabry disease: correlation with renal diseaseTamar Shemesh, Catharina Whybra, Sandra Delgado-Sanchez, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 28, 2008
Cardiac manifestations of Anderson-Fabry disease in children and adolescentsChristoph Kampmann, Christiane M Wiethoff, Catharina Whybra, et al.
Gene|September 24, 2013
Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653-5655delTAT, causing harlequin ichthyosisJohannes Follmann, Doris Macchiella, Catharina Whybra, et al.
Bipolar Disorders|August 2, 2006
Recurrent brief depression in a female patient with Fabry diseaseMatthias J Müller, Andreas Fellgiebel, Armin Scheurich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2009
A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry diseaseCatharina Whybra, Elke Miebach, Eugen Mengel, et al.
Molecular Genetics & Genomic Medicine|March 8, 2020
Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopeniaMascha Schönfeld, Mareike Selig, Alexandra Russo, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Zeitschrift Fur Geburtshilfe Und Neonatologie|June 6, 2020
[Results of the hypothermia registry of the University Hospital Dresden from 2010-2017. Application of hypothermia therapy in newborns in Germany]Jonas Scherer, Catharina Whybra-Trümpler, Eva Mildenberger
Acta Paediatrica (Oslo, Norway : 1992)|March 19, 2020
Non-immune hydrops fetalis was rare in Sweden during 1997-2015, but cases were associated with complications and poor prognosisCatharina Whybra, Karin Källén, Stefan R Hansson, et al.
European Cytokine Network|March 14, 2007
An association study of inflammatory cytokine gene polymorphisms in Fabry diseaseRachael Safyan, Catharina Whybra, Michael Beck, et al.
Klinische Padiatrie|July 19, 2017
Weaning Premature Infants from Nasal Continuous Positive Airway Pressure - Current Practice and Scientific EvidenceAndré Kidszun, Christine Arnold, Julia Winter, et al.
Nephron. Clinical Practice|July 20, 2010
Paraoxonase (PON1) gene polymorphisms in Fabry disease: correlation with renal diseaseTamar Shemesh, Catharina Whybra, Sandra Delgado-Sanchez, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 28, 2008
Cardiac manifestations of Anderson-Fabry disease in children and adolescentsChristoph Kampmann, Christiane M Wiethoff, Catharina Whybra, et al.
Gene|September 24, 2013
Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653-5655delTAT, causing harlequin ichthyosisJohannes Follmann, Doris Macchiella, Catharina Whybra, et al.
Bipolar Disorders|August 2, 2006
Recurrent brief depression in a female patient with Fabry diseaseMatthias J Müller, Andreas Fellgiebel, Armin Scheurich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2009
A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry diseaseCatharina Whybra, Elke Miebach, Eugen Mengel, et al.
Molecular Genetics & Genomic Medicine|March 8, 2020
Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopeniaMascha Schönfeld, Mareike Selig, Alexandra Russo, et al.
Pageof 3