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