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