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