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Chana Vinkler

Showing results (1-10 of 31) with videos related to

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Fetal Diagnosis and Therapy|October 15, 2011
Hemifacial microsomia with spinal and rib anomalies: prenatal diagnosis and postmortem confirmation using 3-D computed tomography reconstructionKarina Haratz, Chana Vinkler, Dorit Lev, et al.
Clinical Pediatrics|October 9, 2002
Congenital cytomegalovirus infection presenting as an apparent neurodegenerative disorderNathan Watemberg, Orna Vardi, Dorit Lev, et al.
The Journal of Pediatrics|January 24, 2007
Congenital patent ductus venosus: an association with the hyper IgE syndromeKeren Sagiv-Friedgut, Michaela Witzling, Ilan Dalal, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 15, 2011
Autistic regression in a child with Silver-Russell syndrome and maternal UPD 7Orna Vardi, Michael Davidovitch, Chana Vinkler, et al.
European Journal of Medical Genetics|April 9, 2014
A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial featuresChana Vinkler, Esther Leshinsky-Silver, Marina Michelson, et al.
Journal of Child Neurology|November 6, 2004
Familial hyperekplexia and refractory status epilepticus: a new autosomal recessive syndromeTally Lerman-Sagie, Nathan Watemberg, Chana Vinkler, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Mosaic marker chromosome 16 resulting in 16q11.2-q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasiaAyelet Zerem, Chana Vinkler, Marina Michelson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2006
A benign congenital myopathy in an inbred Samaritan familyDorit Lev, Menachem Sadeh, Nathan Watemberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2007
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 15, 2010
Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the motherMarina Michelson, Avi Eden, Chana Vinkler, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Fetal Diagnosis and Therapy|October 15, 2011
Hemifacial microsomia with spinal and rib anomalies: prenatal diagnosis and postmortem confirmation using 3-D computed tomography reconstructionKarina Haratz, Chana Vinkler, Dorit Lev, et al.
Clinical Pediatrics|October 9, 2002
Congenital cytomegalovirus infection presenting as an apparent neurodegenerative disorderNathan Watemberg, Orna Vardi, Dorit Lev, et al.
The Journal of Pediatrics|January 24, 2007
Congenital patent ductus venosus: an association with the hyper IgE syndromeKeren Sagiv-Friedgut, Michaela Witzling, Ilan Dalal, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 15, 2011
Autistic regression in a child with Silver-Russell syndrome and maternal UPD 7Orna Vardi, Michael Davidovitch, Chana Vinkler, et al.
European Journal of Medical Genetics|April 9, 2014
A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial featuresChana Vinkler, Esther Leshinsky-Silver, Marina Michelson, et al.
Journal of Child Neurology|November 6, 2004
Familial hyperekplexia and refractory status epilepticus: a new autosomal recessive syndromeTally Lerman-Sagie, Nathan Watemberg, Chana Vinkler, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Mosaic marker chromosome 16 resulting in 16q11.2-q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasiaAyelet Zerem, Chana Vinkler, Marina Michelson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2006
A benign congenital myopathy in an inbred Samaritan familyDorit Lev, Menachem Sadeh, Nathan Watemberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2007
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 15, 2010
Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the motherMarina Michelson, Avi Eden, Chana Vinkler, et al.
Pageof 4