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