Hanna C. Maayan
Jerusalem, JM, Israel
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 23 publications
Addendum to Nociception and pain in humans lacking a functional TRPV1 channel.
Journal: The Journal of clinical investigation
Published: April 01, 2026
Human Mutations in the TRPV1 Channel: Implications for Noxious Cold Sensation.
Journal: Annual review of pharmacology and toxicology
Published: July 09, 2025
Pancreatitis in Familial Dysautonomia Patients.
Journal: Digestive diseases (Basel, Switzerland)
Published: June 15, 2025
Retrograde tubing as a rescue treatment for megaoesophagus: a case report.
Journal: BMJ open gastroenterology
Published: October 25, 2023
Nociception and pain in humans lacking a functional TRPV1 channel.
Journal: The Journal of clinical investigation
Published: July 27, 2021
Uncommon side effects of common drugs in patients with familial dysautonomia.
Journal: Pharmacoepidemiology and drug safety
Published: September 15, 2020
Respiratory care in familial dysautonomia: Systematic review and expert consensus recommendations.
Journal: Respiratory medicine
Published: January 17, 2018
Characteristics of ataxic gait in familial dysautonomia patients.
Journal: PloS one
Published: August 17, 2017
Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia.
Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
Published: August 29, 2016
Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study.
Journal: Journal of molecular neuroscience : MN
Published: February 15, 2016
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: July 10, 2015
Last Updated: 09/26/2026