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