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