There is no disease so rare
that it does not deserve attention

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• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
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• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
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• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
  • More details
• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • IonNeurONet: Molecular diagnosis and exome sequencing in ion channel diseases (project 7)
  • CeGaT GmbH
  • CeGaT GmbH und Praxis für Humangenetik
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• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • Differential physiological and pathophysiological role of neuronal voltage gated Na+ channels Nav1.1 (SCN1A) and Nav1.2 (SCN2A)
  • Hertie-Institut für klinische Hirnforschung
  • Abteilung für Neurologie mit Schwerpunkt Epileptologie
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• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
  • Hertie-Institut für klinische Hirnforschung
  • Abteilung für Neurologie mit Schwerpunkt Epileptologie
  • More details
• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • IonNeurONet: Regulation of surface expression and development of bio assays to improve the situation of patients harbouring a mutation leading to transporter defect in channelopathies (project 6)
  • Universitätsklinik Tübingen
  • Molekulargenetisches Labor
  • More details
• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
  • Universitätsklinikum Tübingen
  • Medizinische Genetik Tübingen
  • More details
• • GERMANY
  • Baden-Württemberg
  • ULM
  • Excitation-contraction coupling in health and disease: Ion channel diseases - diagnosis, pathogenesis and therapy
  • Universität Ulm
  • Institut für Angewandte Physiologie
  • More details
• • GERMANY
  • Baden-Württemberg
  • ULM
  • IonNeurONet: Gene identification and characterisation of hemiplegic migraine (project 4)
  • Universitätsklinikum Ulm
  • Institut für Humangenetik
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• • GERMANY
  • Bayern
  • MÜNCHEN
  • Mutational analysis of CACNA1A, ATP1A2 and SCN1A genes (direct sequencing)
  • LMU Klinikum der Universität München - Campus Großhadern
  • Arbeitsgruppe Neurogenetik
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• • GERMANY
  • Bayern
  • MÜNCHEN
  • Functional characterization of ATP1A2 mutations associated with FHM by cell survival assays
  • LMU Klinikum der Universität München - Campus Großhadern
  • Arbeitsgruppe Neurogenetik
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• • GERMANY
  • Bayern
  • MÜNCHEN
  • Generation of a knock-in mouse model for FHM3
  • LMU Klinikum der Universität München - Campus Großhadern
  • Arbeitsgruppe Neurogenetik
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• • GERMANY
  • Bayern
  • MÜNCHEN
  • Genetics of familial and sporadic hemiplegic migraine (Investigations on CACNA1A, ATP1A2 und SCN1A genes)
  • LMU Klinikum der Universität München - Campus Großhadern
  • Arbeitsgruppe Neurogenetik
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• • GERMANY
  • Bayern
  • MÜNCHEN
  • BNE: BrainNet Europe II: European brain tissue bank - Network for clinical neuroscience and basic research (coordination)
  • Ludwig-Maximilians-Universität München
  • Zentrum für Neuropathologie und Prionforschung
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• • ITALY
  • LOMBARDIA
  • MILANO
  • Genetic and micro-environmental factors regulate the role of atp as transmitter of pain in a migraine model
  • Università degli Studi di Milano
  • Dipartimento di Scienze Farmacologiche
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• • ITALY
  • LOMBARDIA
  • MILANO
  • Studies of familial hemiplegic migraine transgenic mouse models and patients to investigate the crosstalk between sensory neurons and neuroinflammatory cells in trigeminal ganglia in relation to migraine pain.
  • Università degli Studi di Milano
  • Dipartimento di Scienze Farmacologiche
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• • ITALY
  • VENETO
  • PADOVA
  • Functional consequences of mutations associated to familial hemiplegic migraine and migraine mechanisms
  • Università degli Studi di Padova
  • Dipartimento di Scienze Biomediche
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• • NETHERLANDS
  • Zuid-Holland
  • LEIDEN
  • 
  • Migraine genes and neurobiological pathways
  • LUMC - Leids Universitair Medisch Centrum
  • Afdeling Neurologie
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• • PORTUGAL
  • NORTE
  • PORTO
  • CACNA1A gene involvement in cognition and synaptic function in calcium channel disease.
  • Instituto de Biologia Molecular e Celular
  • Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
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• • PORTUGAL
  • NORTE
  • PORTO
  • Search for disease modifiers in spinocerebellar ataxias: human and animal-based approaches.
  • Instituto de Biologia Molecular e Celular
  • Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
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• • SPAIN
  • Cataluña
  • BARCELONA
  • Functional consequences of migraine associated mutations in ion channel activity and neurotransmitter release in familial hemiplegic migraine.
  • Universitat Pompeu Fabra. Facultat de Ciències de la Salut i de la Vida
  • Laboratorio de Fisiología Molecular y Canalopatías
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• • SPAIN
  • Cataluña
  • BARCELONA
  • Genetic basis and Functional studies of episodic neurological channelopathies: migraine and ataxia
  • Universitat de Barcelona. Facultat de Biologia
  • Departamento de Genética
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