Neurodégénérescence associée à la protéine de membrane mitochondriale
All Entries 4
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Coenzyme Q10 deficiency
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Recessive mitochondrial ataxia syndrome
- MERRF
- Barth syndrome
- Mitochondrial myopathy
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- MELAS
- Mitochondrial DNA depletion syndrome
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Leber hereditary optic neuropathy
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Rare ataxia
- COASY protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Myasthenia gravis
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Mitochondrial disease
- Hereditary spastic paraplegia
- Neuroferritinopathy
- Mitochondrial membrane protein-associated neurodegeneration
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Pantothenate kinase-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Care facilities 2
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Coenzyme Q10 deficiency
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Recessive mitochondrial ataxia syndrome
- MERRF
- Barth syndrome
- Mitochondrial myopathy
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- MELAS
- Mitochondrial DNA depletion syndrome
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Leber hereditary optic neuropathy
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Rare ataxia
- COASY protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Myasthenia gravis
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Mitochondrial disease
- Hereditary spastic paraplegia
- Neuroferritinopathy
- Mitochondrial membrane protein-associated neurodegeneration
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Pantothenate kinase-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Infantile neuroaxonal dystrophy
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome