Gabriel Miltenberger-Miltenyi
AuthID: R-000-VAB
21
TITLE: Clinical and Electrophysiological Features in Charcot-Marie-Tooth Disease With Mutations in the NEFL Gene
AUTHORS: Gabriel Miltenberger-Miltenyi; Andreas R Janecke; Julia V Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N Löscher;
PUBLISHED: 2007, SOURCE: Arch Neurol - Archives of Neurology, VOLUME: 64, ISSUE: 7
AUTHORS: Gabriel Miltenberger-Miltenyi; Andreas R Janecke; Julia V Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N Löscher;
PUBLISHED: 2007, SOURCE: Arch Neurol - Archives of Neurology, VOLUME: 64, ISSUE: 7
INDEXED IN: 
CrossRef
CrossRef22
TITLE: Novel C59T leader peptide mutation in the MPZ gene associated with late‐onset, axonal, sensorimotor polyneuropathy
AUTHORS: Finsterer, J; Miltenberger, G; Rauschka, H; Janecke, A;
PUBLISHED: 2006, SOURCE: European Journal of Neurology, VOLUME: 13, ISSUE: 10
AUTHORS: Finsterer, J; Miltenberger, G; Rauschka, H; Janecke, A;
PUBLISHED: 2006, SOURCE: European Journal of Neurology, VOLUME: 13, ISSUE: 10
23
TITLE: Mutation spectrum of type I glycogen storage disease in Hungary Full Text
AUTHORS: Miltenberger Miltenyi, G; Szonyi, L; Balogh, L; Utermann, G; Janecke, AR;
PUBLISHED: 2005, SOURCE: Journal of Inherited Metabolic Disease, VOLUME: 28, ISSUE: 6
AUTHORS: Miltenberger Miltenyi, G; Szonyi, L; Balogh, L; Utermann, G; Janecke, AR;
PUBLISHED: 2005, SOURCE: Journal of Inherited Metabolic Disease, VOLUME: 28, ISSUE: 6
INDEXED IN: 
Scopus
Scopus24
TITLE: Mutation spectrum of type I glycogen storage disease in Hungary Full Text
AUTHORS: Miltenberger-Miltenyi, G; Szonyi, L; Balogh, L; Utermann, G; Janecke, AR;
PUBLISHED: 2005, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 28, ISSUE: 6
AUTHORS: Miltenberger-Miltenyi, G; Szonyi, L; Balogh, L; Utermann, G; Janecke, AR;
PUBLISHED: 2005, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 28, ISSUE: 6
25
TITLE: Primary pulmonary hypertension in children may have a different genetic background than in adults
AUTHORS: Grunig, E; Koehler, R; Miltenberger Miltenyi, G; Zimmermann, R; Gorenflo, M; Mereles, D; Arnold, K; Naust, B; Wilkens, H; Benz, A; Von Hippel, A; Ulmer, HE; Kubler, W; Katus, HA; Bartram, CR; Schranz, D; Janssen, B;
PUBLISHED: 2004, SOURCE: Pediatric Research, VOLUME: 56, ISSUE: 4
AUTHORS: Grunig, E; Koehler, R; Miltenberger Miltenyi, G; Zimmermann, R; Gorenflo, M; Mereles, D; Arnold, K; Naust, B; Wilkens, H; Benz, A; Von Hippel, A; Ulmer, HE; Kubler, W; Katus, HA; Bartram, CR; Schranz, D; Janssen, B;
PUBLISHED: 2004, SOURCE: Pediatric Research, VOLUME: 56, ISSUE: 4
INDEXED IN: Scopus
Scopus26
TITLE: Primary Pulmonary Hypertension in Children May Have a Different Genetic Background Than in Adults
AUTHORS: Ekkehard Grünig; Rolf Koehler; Gabriel Miltenberger-Miltenyi; Rainer Zimmermann; Matthias Gorenflo; Derliz Mereles; Karlin Arnold; Barbara Naust; Heinrike Wilkens; Andreas Benz; Albrecht von Hippel; Herbert E Ulmer; Wolfgang Kübler; Hugo A Katus; Claus R Bartram; Dietmar Schranz; Bart Janssen;
PUBLISHED: 2004, SOURCE: Pediatr Res - Pediatric Research, VOLUME: 56, ISSUE: 4
AUTHORS: Ekkehard Grünig; Rolf Koehler; Gabriel Miltenberger-Miltenyi; Rainer Zimmermann; Matthias Gorenflo; Derliz Mereles; Karlin Arnold; Barbara Naust; Heinrike Wilkens; Andreas Benz; Albrecht von Hippel; Herbert E Ulmer; Wolfgang Kübler; Hugo A Katus; Claus R Bartram; Dietmar Schranz; Bart Janssen;
PUBLISHED: 2004, SOURCE: Pediatr Res - Pediatric Research, VOLUME: 56, ISSUE: 4
27
TITLE: Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31 Full Text
AUTHORS: Rindermann, M; Grunig, E; Von Hippel, A; Koehler, R; Miltenberger Miltenyi, G; Mereles, D; Arnold, K; Pauciulo, M; Nichols, W; Olschewski, H; Hoeper, MM; Winkler, J; Katus, HA; Kubler, W; Bartram, CR; Janssen, B;
PUBLISHED: 2003, SOURCE: Journal of the American College of Cardiology, VOLUME: 41, ISSUE: 12
AUTHORS: Rindermann, M; Grunig, E; Von Hippel, A; Koehler, R; Miltenberger Miltenyi, G; Mereles, D; Arnold, K; Pauciulo, M; Nichols, W; Olschewski, H; Hoeper, MM; Winkler, J; Katus, HA; Kubler, W; Bartram, CR; Janssen, B;
PUBLISHED: 2003, SOURCE: Journal of the American College of Cardiology, VOLUME: 41, ISSUE: 12
28
TITLE: Mutations and polymorphisms in the human methyl CpG-binding protein MECP2 Full Text
AUTHORS: Miltenberger Miltenyi, G; Laccone, F;
PUBLISHED: 2003, SOURCE: Human Mutation, VOLUME: 22, ISSUE: 2
AUTHORS: Miltenberger Miltenyi, G; Laccone, F;
PUBLISHED: 2003, SOURCE: Human Mutation, VOLUME: 22, ISSUE: 2
INDEXED IN: Scopus
Scopus29
TITLE: Mutations and polymorphisms in the human methyl CpG-binding protein MECP2 Full Text
AUTHORS: Gabriel Miltenberger-Miltenyi; Franco Laccone;
PUBLISHED: 2003, SOURCE: Human Mutation - Hum. Mutat., VOLUME: 22, ISSUE: 2
AUTHORS: Gabriel Miltenberger-Miltenyi; Franco Laccone;
PUBLISHED: 2003, SOURCE: Human Mutation - Hum. Mutat., VOLUME: 22, ISSUE: 2
30
TITLE: Primary pulmonary hypertension is predominantly a hereditary disease Full Text
AUTHORS: Grunig, E; Mereles, D; Arnold, K; Benz, A; Olschewski, H; Miltenberger Miltenyi, G; Borst, MM; Abushi, A; Seeger, W; Winkler, J; Hoper, MM; Bartram, CR; Kubler, W; Janssen, B;
PUBLISHED: 2002, SOURCE: Chest, VOLUME: 121, ISSUE: 3
AUTHORS: Grunig, E; Mereles, D; Arnold, K; Benz, A; Olschewski, H; Miltenberger Miltenyi, G; Borst, MM; Abushi, A; Seeger, W; Winkler, J; Hoper, MM; Bartram, CR; Kubler, W; Janssen, B;
PUBLISHED: 2002, SOURCE: Chest, VOLUME: 121, ISSUE: 3
INDEXED IN: Scopus
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ORCID
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