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Daniela Karall

Showing results (11-20 of 129) with videos related to

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Neuropediatrics|April 5, 2012
Unrecognized citrullinemia mimicking encephalitis in a 14-year-old boy: unexpected result through the use of a standardized lumbar puncture protocolDaniela Karall, Edda Haberlandt, Ursula Albrecht, et al.
European Journal of Medical Genetics|September 21, 2007
Homozygosity for MECP2 gene in a girl with classical Rett syndromeDaniela Karall, Edda Haberlandt, Sabine Scholl-Bürgi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2012
Recurrent somnolence in a 17-month-old infant: late-onset ornithine transcarbamylase (OTC) deficiency due to the novel hemizygous mutation c.535C > T (p.Leu179Phe)Michaela Fantur, Daniela Karall, Sabine Scholl-Buergi, et al.
Studies in Health Technology and Informatics|May 12, 2026
GenKom-PKU: Improving Patient-Provider Communication in PhenylketonuriaMoritz Henninger, Alexander Höller, Daniela Karall, et al.
Neuropediatrics|July 7, 2021
Subdural Hygroma in an Infant with Marfan's SyndromeLisa Ballmann, Sabine Scholl-Bürgi, Thomas Karall, et al.
Archives of Oral Biology|May 6, 2017
Variable expressivity of TCTEX1D2 mutations and a possible pathogenic link of molar-incisor malformation to ciliary dysfunctionJohannes Zschocke, Anna Schossig, Dieter D Bosshardt, et al.
Journal of Breath Research|May 16, 2018
Breath profiles of children on ketogenic therapyVeronika Ruzsányi, Miklós Péter Kalapos, Christine Schmidl, et al.
Molecular Genetics & Genomic Medicine|January 20, 2021
Characteristic facial features and cortical blindness distinguish the DOCK7-related epileptic encephalopathyEdda Haberlandt, Taras Valovka, Tanja Janjic, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 11, 2019
Frenotomy for tongue-tie (frenulum linguae breve) showed improved symptoms in the short- and long-term follow-upGabriele Ramoser, Márta Guóth-Gumberger, Sara Baumgartner-Sigl, et al.
Epilepsy Research|January 15, 2013
Matrix-metalloproteinases and proinflammatory cytokines in children with febrile convulsions and epilepsy--cause or consequence?Edda Haberlandt, Markus Rauchenzauner, Maike Morass, et al.
Pageof 13

Showing results (11-20 of 129) with videos related to

Sort By:
Pageof 13
Neuropediatrics|April 5, 2012
Unrecognized citrullinemia mimicking encephalitis in a 14-year-old boy: unexpected result through the use of a standardized lumbar puncture protocolDaniela Karall, Edda Haberlandt, Ursula Albrecht, et al.
European Journal of Medical Genetics|September 21, 2007
Homozygosity for MECP2 gene in a girl with classical Rett syndromeDaniela Karall, Edda Haberlandt, Sabine Scholl-Bürgi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2012
Recurrent somnolence in a 17-month-old infant: late-onset ornithine transcarbamylase (OTC) deficiency due to the novel hemizygous mutation c.535C > T (p.Leu179Phe)Michaela Fantur, Daniela Karall, Sabine Scholl-Buergi, et al.
Studies in Health Technology and Informatics|May 12, 2026
GenKom-PKU: Improving Patient-Provider Communication in PhenylketonuriaMoritz Henninger, Alexander Höller, Daniela Karall, et al.
Neuropediatrics|July 7, 2021
Subdural Hygroma in an Infant with Marfan's SyndromeLisa Ballmann, Sabine Scholl-Bürgi, Thomas Karall, et al.
Archives of Oral Biology|May 6, 2017
Variable expressivity of TCTEX1D2 mutations and a possible pathogenic link of molar-incisor malformation to ciliary dysfunctionJohannes Zschocke, Anna Schossig, Dieter D Bosshardt, et al.
Journal of Breath Research|May 16, 2018
Breath profiles of children on ketogenic therapyVeronika Ruzsányi, Miklós Péter Kalapos, Christine Schmidl, et al.
Molecular Genetics & Genomic Medicine|January 20, 2021
Characteristic facial features and cortical blindness distinguish the DOCK7-related epileptic encephalopathyEdda Haberlandt, Taras Valovka, Tanja Janjic, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 11, 2019
Frenotomy for tongue-tie (frenulum linguae breve) showed improved symptoms in the short- and long-term follow-upGabriele Ramoser, Márta Guóth-Gumberger, Sara Baumgartner-Sigl, et al.
Epilepsy Research|January 15, 2013
Matrix-metalloproteinases and proinflammatory cytokines in children with febrile convulsions and epilepsy--cause or consequence?Edda Haberlandt, Markus Rauchenzauner, Maike Morass, et al.
Pageof 13