Mitochondrial membrane protein-associated neurodegeneration
All Entries 4
Friedrich-Baur-Institut der Neurologischen Klinik, am LMU Klinikum München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Page Web
Email
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Huntington disease
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
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Coenzyme Q10 deficiency
- Kearns-Sayre syndrome
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- MELAS
- Barth syndrome
- Mitochondrial myopathy
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
Trogerstr. 32
81675 München
089 41406381
089 41406382
Page Web
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Syndrome de Kufor-Rakeb
- Neurodégénérescence associée à FA2H
- Aceruloplasminemia
- Paraplégie spastique autosomique récessive type 35
- Infantile neuroaxonal dystrophy
- Dystonie-parkinsonisme de l'adulte
- Neurodégénérescence associée à la protéine COASY
- Neuroferritinopathy
- PLA2G6-associated neurodegeneration
- Neurodégénérescence par déficit en pantothénate kinase
- Beta-propeller protein-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodégénérescence avec surcharge cérébrale en fer
Institutions de rang supérieur 0
Conseil génétique 1
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
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 440057470
089 440057402
Page Web
Email
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Huntington disease
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
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Coenzyme Q10 deficiency
- Kearns-Sayre syndrome
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- MELAS
- Barth syndrome
- Mitochondrial myopathy
Associations de patients 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Syndrome de Kufor-Rakeb
- Neurodégénérescence associée à FA2H
- Aceruloplasminemia
- Paraplégie spastique autosomique récessive type 35
- Infantile neuroaxonal dystrophy
- Dystonie-parkinsonisme de l'adulte
- Neurodégénérescence associée à la protéine COASY
- Neuroferritinopathy
- PLA2G6-associated neurodegeneration
- Neurodégénérescence par déficit en pantothénate kinase
- Beta-propeller protein-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodégénérescence avec surcharge cérébrale en fer