Home › Researcher directory › Daniel Hantaı̈
Daniel Hantaı̈
Affiliation : Inserm · Assistance Publique – Hôpitaux de Paris · Pitié-Salpêtrière Hospital · Institut du Cerveau
- 8Publications (affiliation in France)
- 128Total publications
- 3837Citations
- 34h-index
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Create my free profile Add my publicationsResearch areas
- Muscle Physiology and Disorders
- Myasthenia Gravis and Thymoma
- Neurogenetic and Muscular Disorders Research
- Protease and Inhibitor Mechanisms
- Blood Coagulation and Thrombosis Mechanisms
Publications (8)
- A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia
- Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia
- Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia
- Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing
- Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function
- Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
- Remaniements expérimentaux et pathologiques de la jonction neuromusculaire
- Developmental Regulation of Amyloid Precursor Protein at the Neuromuscular Junction in Mouse Skeletal Muscle
Co-authors
- B. Eymard
- Pascale Richard
- Karen Gaudon
- Jeanine Koenig
- Michel Fardeau
- Stéphanie Bauché
- Evelyne Goillot
- Laurent Schaeffer
- Caroline Huzé
- Jean‐Paul Leroy
- Payam Soltanzadeh
- Antoine Taly
Bibliographic data from OpenAlex (open database).
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