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 440057400
089 440057402
Page Web
Email
- Atypical pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Neuroferritinopathy
- Mitochondrial disease
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- COASY protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
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
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Coenzyme Q10 deficiency
- Leber hereditary optic neuropathy
- Pearson syndrome
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- MELAS
- Mitochondrial DNA depletion syndrome
- Recessive mitochondrial ataxia syndrome
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Barth syndrome
- Mitochondrial myopathy
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
- Neuroferritinopathy
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Autosomal recessive spastic paraplegia type 35
- Aceruloplasminemia
- Infantile neuroaxonal dystrophy
- Pantothenate kinase-associated neurodegeneration
- Fatty acid hydroxylase-associated neurodegeneration
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
- Atypical pantothenate kinase-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Neuroferritinopathy
- Mitochondrial disease
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- COASY protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
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
- Kearns-Sayre syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Coenzyme Q10 deficiency
- Leber hereditary optic neuropathy
- Pearson syndrome
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- MELAS
- Mitochondrial DNA depletion syndrome
- Recessive mitochondrial ataxia syndrome
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Barth syndrome
- Mitochondrial myopathy
Associations de patients 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Neuroferritinopathy
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Autosomal recessive spastic paraplegia type 35
- Aceruloplasminemia
- Infantile neuroaxonal dystrophy
- Pantothenate kinase-associated neurodegeneration
- Fatty acid hydroxylase-associated neurodegeneration