-Ute Hehr Researcher Activity Profile

Research Author Detailed Information 

Ute Hehr Publication Rate By Year

Ute Hehr has published 4 paper(s) in 2004, 2 paper(s) in 2006, 3 paper(s) in 2007, 3 paper(s) in 2008, for a total of 12 research publications in total.

Ute U Hehr Author Information

LAST NAME: hehr

FIRST NAME: Ute

INITIALS: u

AFFILIATION:

Papers

Ute Hehr's Publication Record

1. Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease. Year Published: 2007
2. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene. Year Published: 2004
Center for Pediatrics and Human Genetics, Hannover Medical School, Hannover, Germany. hartmann.hans@mh-hannover.de
3. X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting. Year Published: 2004
Department of Neuropediatrics, University of Giessen, Giessen, Germany. Andreas.Hahn@paediat.med.uni-giessen.de
4. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Year Published: 2006
Department of Pediatric Neurology, Hacettepe University, Ankara, Turkey.
5. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Year Published: 2008
Department of Human Genetics, University of Regensburg, Regensburg.
6. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Year Published: 2008
Department of Human Genetics, University of Regensburg, Regensburg, Germany.
7. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene. Year Published: 2004
Center for Pediatrics and Human Genetics, Hannover Medical School, Hannover, Germany. hartmann.hans@mh-hannover.de
8. X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting. Year Published: 2004
Department of Neuropediatrics, University of Giessen, Giessen, Germany. Andreas.Hahn@paediat.med.uni-giessen.de
9. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Year Published: 2006
Department of Pediatric Neurology, Hacettepe University, Ankara, Turkey.
10. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Year Published: 2008
Department of Human Genetics, University of Regensburg, Regensburg, Germany.
11. Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease. Year Published: 2007
Center for Human Genetics and Department of Human Genetics, University of Regensburg, Universitätklinikum D3, Franz-Josef-Strauss-Allee 11, Regensburg 93053, Germany. info@humangenetik-regensburg.de
12. Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease. Year Published: 2007