se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg

Decription of facility

Director / Spokesperson
Prof. Dr. J. Volkmann
Information
Care facility for adults and children
Decription

Die Neurologie hat sich in den letzten 20 Jahren von einem diagnostischen zu einem therapeutischen Fach gewandelt. Schlaganfall, multiple Sklerose, Parkinson-Krankheit, Epilepsien, Nerven- und Muskelerkrankungen sind heute vielfältig behandelbar. Die neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg bietet Diagnostik und Therapie nach modernsten Standards auf dem gesamten Gebiet der Neurologie an.

In zahlreichen Spezialsprechstunden sowie im Rahmen konsiliarischer Untersuchungen werden jährlich fast 11 000 Patientinnen und Patienten behandelt. 3400 werden stationär aufgenommen, davon über 500 intensivmedizinisch. Bei einem Großteil der stationären Aufnahmen handelt es sich um Notfälle, die in der neurologisch-neurochirurgischen Notaufnahme erstversorgt werden. Die Klinik verfügt über 86 Planbetten, darunter acht auf der Stroke Unit und zehn auf der klinikeigenen Intensivstation. Gemeinsam mit dem Zentrum für Psychische Gesundheit wird eine neurogerontopsychiatrische Tagesklinik betrieben, in der bis zu 18 Patientinnen und Patienten mit neuropsychiatrischen Störungen wie etwa Morbus Parkinson interdisziplinär behandelt werden können.

In die Klinik integriert sind die Abteilung für Experimentelle Entwicklungsneurobiologie mit Elektronenmikroskopie und das Liquorlabor.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat Annegret Hauck
0931 20123751
hauck_a3@ukw.de
Website

http://www.neurologie.ukw.de

Address

Josef-Schneider-Straße 2
97080 Würzburg

Hauptareal des Universitätsklinikums, Bereich B (Haus B1)

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Mentioned by the following facilities 1

Preview of the assigned diseases 7

Autosomal recessive distal hereditary motor neuropathy Brain inflammatory disease Congenital lethal myopathy, Compton-North type Laminin subunit alpha 2-related congenital muscular dystrophy Progressive hemifacial atrophy Fingerprint body myopathy Muscular channelopathy Isaac syndrome Distal hereditary motor neuropathy type 1 Spheroid body myopathy Emery-Dreifuss muscular dystrophy Autosomal dominant congenital benign spinal muscular atrophy Distal myopathy with posterior leg and anterior hand involvement Huntington disease Duchenne and Becker muscular dystrophy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Rippling muscle disease Limb-girdle muscular dystrophy Niemann-Pick disease type C, adult neurologic onset Acute disseminated encephalomyelitis Zebra body myopathy Reducing body myopathy Proximal spinal muscular atrophy type 1 Juvenile amyotrophic lateral sclerosis Native American myopathy Corpus callosum agenesis-neuronopathy syndrome Skeletal muscle disease Facioscapulohumeral dystrophy Rigid spine syndrome Morvan syndrome Oculopharyngeal muscular dystrophy Distal hereditary motor neuropathy type 2 Myxofibrosarcoma Hypokalemic periodic paralysis Muscular dystrophy Congenital myopathy Infantile myofibromatosis Parkinson-dementia complex of Guam Progressive supranuclear palsy Tubular aggregate myopathy Juvenile polymyositis Paramyotonia congenita of Von Eulenburg Genetic skeletal muscle disease Distal myopathy with anterior tibial onset Hereditary spastic paraplegia Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Muscle filaminopathy Distal hereditary motor neuropathy type 5 Logopenic progressive aphasia KLHL9-related early-onset distal myopathy Acquired skeletal muscle disease Idiopathic inflammatory myopathy Congenital muscular dystrophy, Ullrich type Frontotemporal dementia Progressive muscular dystrophy Distal anoctaminopathy Metabolic myopathy Congenital muscular dystrophy with integrin alpha-7 deficiency Neuromuscular junction disease Distal myopathy with early respiratory muscle involvement Myotonic dystrophy Autosomal recessive distal myopathy Congenital muscular dystrophy with hyperlaxity Hereditary continuous muscle fiber activity Distal nebulin myopathy Tel Hashomer camptodactyly syndrome Brody myopathy Genetic neuromuscular junction disease Autosomal dominant distal myopathy Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Distal spinal muscular atrophy type 3 Distal hereditary motor neuropathy, Jerash type Classic progressive supranuclear palsy syndrome Non-dystrophic myopathy Distal myotilinopathy Inclusion myopathy X-linked distal spinal muscular atrophy type 3 Alpha-crystallinopathy Vogt-Koyanagi-Harada disease Eosinophilic fasciitis Late-onset distal myopathy, Markesbery-Griggs type Motor neuron disease Synaptic congenital myasthenic syndromes Congenital muscular dystrophy due to LMNA mutation Acquired motor neuron disease Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Miyoshi myopathy Genetic motor neuron disease Cylindrical spirals myopathy Inflammatory myopathy with abundant macrophages Myotonia fluctuans Genetic periodic paralysis Acetazolamide-responsive myotonia Progressive supranuclear palsy-parkinsonism syndrome Myopathy with hexagonally cross-linked tubular arrays Spinal muscular atrophy with respiratory distress type 1 King-Denborough syndrome Autosomal dominant proximal spinal muscular atrophy Fatal post-viral neurodegenerative disorder Myasthenia gravis Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Adult-onset myasthenia gravis Trichinellosis Andersen-Tawil syndrome Macrophagic myofasciitis Myofibrillar myopathy Atypical progressive supranuclear palsy syndrome Hereditary inclusion body myopathy type 4 Poliomyelitis Centronuclear myopathy Neuromuscular disease Polymyositis Muscular lipidosis Progressive supranuclear palsy-corticobasal syndrome Juvenile primary lateral sclerosis Muscular glycogenosis Infantile-onset X-linked spinal muscular atrophy Alveolar rhabdomyosarcoma Inclusion body myopathy with Paget disease of bone and frontotemporal dementia GNE myopathy Distal myopathy, Welander type Guillain-Barré syndrome Juvenile myasthenia gravis Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Proximal myotonic myopathy Stiff person spectrum disorder Nemaline myopathy X-linked myopathy with postural muscle atrophy Tibial muscular dystrophy Bethlem myopathy X-linked myopathy with excessive autophagy Early-onset autosomal dominant Alzheimer disease Inclusion body myositis Fetal akinesia-cerebral and retinal hemorrhage syndrome Hereditary myopathy with early respiratory failure Infantile-onset ascending hereditary spastic paralysis Myotonic syndrome Sporadic Creutzfeldt-Jakob disease Intellectual disability-myopathy-short stature-endocrine defect syndrome Chronic inflammatory demyelinating polyneuropathy Congenital myasthenic syndromes with glycosylation defect Thomsen and Becker disease Periodic paralysis Autosomal dominant spastic paraplegia type 17 Proximal spinal muscular atrophy Pontocerebellar hypoplasia type 1 Overlap myositis Muscular tumor Bulbospinal muscular atrophy of adult Congenital fibrosis of extraocular muscles CLIPPERS Behavioral variant of frontotemporal dementia Postpoliomyelitis syndrome Laing early-onset distal myopathy Monomelic amyotrophy Rippling muscle disease with myasthenia gravis Generalized bulbospinal muscular atrophy Antisynthetase syndrome CANOMAD syndrome Autosomal recessive lower motor neuron disease with childhood onset Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 4 Infectious, fungal or parasitic myopathy Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Dermatomyositis Bacterial myositis Early-onset myopathy with fatal cardiomyopathy Viral myositis Focal myositis Parasitic myositis Primary lateral sclerosis Opsoclonus-myoclonus syndrome Frontotemporal dementia with motor neuron disease Progressive non-fluent aphasia Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG Juvenile overlap myositis Semantic dementia Primary progressive aphasia Friedreich ataxia Hyaline body myopathy Fungal myositis Griscelli syndrome type 1 Juvenile idiopathic inflammatory myopathy Myosclerosis Posterior cortical atrophy Niemann-Pick disease type C Multiple sclerosis variant Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Schilder disease Muscular dystrophy-white matter spongiosis syndrome Amyotrophic lateral sclerosis type 4 Young adult-onset distal hereditary motor neuropathy Niemann-Pick disease type C, severe perinatal form Juvenile dermatomyositis Metabolic myopathy due to lactate transporter defect Benign Samaritan congenital myopathy Spinal muscular atrophy associated with central nervous system anomaly Congenital muscular dystrophy due to dystroglycanopathy Congenital fiber-type disproportion myopathy Lower motor neuron syndrome with late-adult onset Niemann-Pick disease type C, severe early infantile neurologic onset Madras motor neuron disease Autosomal dominant adult-onset proximal spinal muscular atrophy Marburg acute multiple sclerosis Rare neuroinflammatory or neuroimmunological disease Niemann-Pick disease type C, juvenile neurologic onset Baló concentric sclerosis Desmin-related myopathy with Mallory body-like inclusions Alpha-B crystallin-related late-onset myopathy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Megaconial congenital muscular dystrophy Niemann-Pick disease type C, late infantile neurologic onset Amyloidosis Hereditary myopathy with lactic acidosis due to ISCU deficiency Congenital myotonia Arthrogryposis due to muscular dystrophy Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant distal hereditary motor neuropathy Frontotemporal degeneration with dementia Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Thyrotoxic periodic paralysis Steinert myotonic dystrophy Idiopathic camptocormia Distal hereditary motor neuropathy type 7 Transient neonatal myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Myotonia permanens Malignant hyperthermia of anesthesia Embryonal rhabdomyosarcoma DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy ATTRV30M amyloidosis Pontocerebellar hypoplasia type 2 Kennedy disease Familial hemophagocytic lymphohistiocytosis Neuromyelitis optica spectrum disorder Congenital muscular dystrophy type 1B Congenital myasthenic syndrome Oculopharyngodistal myopathy Distal myopathy Vocal cord and pharyngeal distal myopathy Congenital myopathy with excess of thin filaments Desminopathy Postsynaptic congenital myasthenic syndromes Presynaptic congenital myasthenic syndromes Potassium-aggravated myotonia Congenital myopathy, Paradas type Hyperkalemic periodic paralysis Muscular dystrophy, Selcen type Finnish upper limb-onset distal myopathy Immune-mediated necrotizing myopathy Adult-onset distal myopathy due to VCP mutation Rare dystonia Rhabdomyosarcoma Schwartz-Jampel syndrome Amyotrophic lateral sclerosis Non-dystrophic myopathy with collagen 6 anomaly Autosomal recessive myogenic arthrogryposis multiplex congenita Cap myopathy Bulbospinal muscular atrophy Bulbospinal muscular atrophy of childhood IgG4-related pachymeningitis Idiopathic eosinophilic myositis Congenital myopathy with cores Autosomal dominant childhood-onset proximal spinal muscular atrophy Riboflavin transporter deficiency Congenital muscular dystrophy Frontotemporal dementia, right temporal atrophy variant Encephalitis

Provided care options 6

# Contact person
1
Myasthenie-Sprechstunde
Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo ab 13:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

2
Spezialambulanz für Bewegungsstörungen
Dr. Chi Wang Ip

0931 20123768
Email
Website
Di ab 8:45 Uhr und Mi ab 11:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

3
Spezialambulanz für Motoneuron-Erkrankungen
Dr. D. Zeller

0931 20123768
Email
Website
Di ab 12:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

4
Spezialambulanz für Multiple Sklerose und andere entzündliche ZNS-Erkrankungen
Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo - Fr ab 8:00 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

5
Spezialambulanz für seltene Gedächtnisstörungen
Dr. Jentschke

0931 20123768
Email
Website
Do ab 13:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

6
Sprechstunde für neuromuskuläre Erkrankungen
Prof. Dr. C. Sommer, Prof. Dr. G. Stoll

0931 20123768
Email
Website
Mo ab 8:30 Uhr, Sprechzeiten nach Vereinbarung. Telefonische Terminvereinbarung Mo - Do 13:30 - 16:00 Uhr

9.953800749.8007685Neurologische Klinik und Poliklinik am Universitätsklinikum Würzburg
Last updated: 15.06.2021