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Maike F Dohrn

Showing results (31-40 of 58) with videos related to

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Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Channels (Austin, Tex.)|January 25, 2021
Assessing the impact of pain-linked Nav1.7 variants: An example of two variants with no biophysical effectKim Le Cann, Jannis E Meents, Vishal Sudha Bhagavath Eswaran, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Neurological Research and Practice|February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibersMaike F Dohrn, Corina Heller, Diana Zengeler, et al.
Journal of Neurology|October 9, 2013
Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathyMaike F Dohrn, Christoph Röcken, Jan L De Bleecker, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neuropediatrics|April 28, 2025
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic PainAnnegret Quade, Annette Lischka, Simone Albani, et al.
European Journal of Neurology|March 7, 2022
RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxiaDanique Beijer, Maike F Dohrn, Jonathan De Winter, et al.
Regional Anesthesia and Pain Medicine|September 22, 2025
Phentolamine selectively blocks C-fiber conduction in different species, including humansSven Christian Engler, Stanislav Koulchitsky, Andelain Erickson, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Channels (Austin, Tex.)|January 25, 2021
Assessing the impact of pain-linked Nav1.7 variants: An example of two variants with no biophysical effectKim Le Cann, Jannis E Meents, Vishal Sudha Bhagavath Eswaran, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Neurological Research and Practice|February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibersMaike F Dohrn, Corina Heller, Diana Zengeler, et al.
Journal of Neurology|October 9, 2013
Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathyMaike F Dohrn, Christoph Röcken, Jan L De Bleecker, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neuropediatrics|April 28, 2025
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic PainAnnegret Quade, Annette Lischka, Simone Albani, et al.
European Journal of Neurology|March 7, 2022
RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxiaDanique Beijer, Maike F Dohrn, Jonathan De Winter, et al.
Regional Anesthesia and Pain Medicine|September 22, 2025
Phentolamine selectively blocks C-fiber conduction in different species, including humansSven Christian Engler, Stanislav Koulchitsky, Andelain Erickson, et al.
Pageof 6