Neurodégénérescence associée à la protéine de membrane mitochondriale
All Entries 4
Friedrich-Baur-Institut der Neurologischen Klinik, am LMU Klinikum München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Page Web
Email
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Beta-propeller protein-associated neurodegeneration
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Myasthenia gravis
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
Page Web
Email
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Recessive mitochondrial ataxia syndrome
- MERRF
- Barth syndrome
- Coenzyme Q10 deficiency
- Mitochondrial myopathy
- Leber hereditary optic neuropathy
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Kearns-Sayre syndrome
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
Page Web
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Neurodegeneration with brain iron accumulation
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Neurodégénérescence associée à la protéine COASY
- Fatty acid hydroxylase-associated neurodegeneration
- Dystonie-parkinsonisme de l'adulte
- Neuroferritinopathy
Institutions de rang supérieur 0
Conseil génétique 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
Page Web
Email
Institutions de prise en charge 2
Friedrich-Baur-Institut der Neurologischen Klinik, am LMU Klinikum München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Page Web
Email
- Mitochondrial membrane protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Beta-propeller protein-associated neurodegeneration
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Leukodystrophy
- Atypical pantothenate kinase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Myasthenia gravis
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
Page Web
Email
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Recessive mitochondrial ataxia syndrome
- MERRF
- Barth syndrome
- Coenzyme Q10 deficiency
- Mitochondrial myopathy
- Leber hereditary optic neuropathy
- Mitochondrial membrane protein-associated neurodegeneration
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Kearns-Sayre syndrome
Associations de patients 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Neurodegeneration with brain iron accumulation
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Neurodégénérescence associée à la protéine COASY
- Fatty acid hydroxylase-associated neurodegeneration
- Dystonie-parkinsonisme de l'adulte
- Neuroferritinopathy