Results 91 to 100 of about 5,298 (208)

A RETREG1 variant is associated with hereditary sensory and autonomic neuropathy with acral self‐mutilation in purebred German Spitz

Animal Genetics, Volume 55, Issue 6, Page 810-819, December 2024.
Abstract Hereditary sensory and autonomic neuropathies (HSAN) represent a group of genetic diseases affecting the peripheral nervous system. In humans, at least 16 loci have been associated with the disorder but do not explain the disease origin of all patients.
Anna Letko, Pascale Quignon, Maéva Quilleré, Jean‐Charles Husson, Caroline Dufaure de Citres, Jonas Donner, Stéphane Dréano, Jocelyn Plassais, Catherine André   +8 more
wiley   +1 more source

"Congenital Sensory Neuropathy as a Differential Diagnosis for Phagocytic Immunodeficiency "

Iranian Journal of Allergy, Asthma and Immunology, 2006
There are few reports about congenital indifference to pain or Hereditary and Sensory Autonomic Neuropathy (HSAN). Several investigations for pathophysiology of this syndrome have been performed and different classifications about it.
Mohammad Gharagozlou, Fariborz Zieh, Parviz Tabatabaei, Gholamreza Zamani   +3 more
doaj  

A p75 neurotrophin receptor‐sparing nerve growth factor protects retinal ganglion cells from neurodegeneration by targeting microglia

British Journal of Pharmacology, Volume 181, Issue 23, Page 4890-4919, December 2024.
Abstract Background and Purpose Retinal ganglion cells (RGCs) are the output stage of retinal information processing, via their axons forming the optic nerve (ON). ON damage leads to axonal degeneration and death of RGCs, and results in vision impairment. Nerve growth factor (NGF) signalling is crucial for RGC operations and visual functions.
Laura Latini, Daniel Souza Monteiro De Araujo, Rosario Amato, Alessio Canovai, Lucia Buccarello, Francesco De Logu, Elena Novelli, Anastasiia Vlasiuk, Francesca Malerba, Ivan Arisi, Rita Florio, Hiroki Asari, Simona Capsoni, Enrica Strettoi, Gino Villetti, Bruno Pietro Imbimbo, Massimo Dal Monte, Romina Nassini, Pierangelo Geppetti, Silvia Marinelli, Antonino Cattaneo   +20 more
wiley   +1 more source

Nonlinear system identification and control using state transition algorithm

, 2015
By transforming identification and control for nonlinear system into optimization problems, a novel optimization method named state transition algorithm (STA) is introduced to solve the problems.
Alfi, Aliprantis, Alireza, Astrom, Chang, Chen, Chunhua Yang, Clerc, Fei, Goldberg, Holland, Kömürcü, Li, Li, Li, Marion, Modares, Seng, Shi, Shinskey, Valarmathi, Weihua Gui, Xiaojun Zhou, Zhou, Zhou   +24 more
core   +1 more source

Pain in Multiple System Atrophy: A Community‐Based Survey

Movement Disorders, Volume 39, Issue 10, Page 1784-1798, October 2024.
Abstract Background Pain is a frequent yet poorly characterized symptom of multiple system atrophy (MSA). Understanding the factors influencing pain and its burden is crucial for improving the symptomatic treatment and quality of life of MSA individuals.
Nicole Campese, Georg Göbel, Julia Wanschitz, Andreas Schlager, Bianca Caliò, Fabian Leys, Pam Bower, Larry Kellerman, Laura Zamarian, Kirsty Bannister, Kallol Ray Chaudhuri, Anette Schrag, Roy Freeman, Horacio Kaufmann, Roberta Granata, Stefan Kiechl, Werner Poewe, Klaus Seppi, Gregor Wenning, Alessandra Fanciulli   +19 more
wiley   +1 more source

Congenital insensitivity to pain: Case report of a rare entity

Indian Journal of Paediatric Dermatology, 2018
Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by insensitivity to noxious stimuli and autonomic dysfunction, associated with pathological abnormalities of the peripheral nerves.
Swati Dahiya, Kondajji Ramchandra Vijayalakshmi, Mubeen Khan   +2 more
doaj   +1 more source

The effects of communication on job satisfaction: an ampiric study in a firm [PDF]

, 2005
Bu araştırmada, yönetici ile işgören arasındaki iletişim düzeyinin iş tatmini üzerindeki etkileri incelenmeye çalışılmıştır. Araştırmanın amacı doğrultusunda geliştirilen üç hipotez test edilmiştir.
Yüksel, İhsan
core  

TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine

American Journal of Medical Genetics Part A, Volume 194, Issue 7, July 2024.
Abstract Due to the majority of currently available genome data deriving from individuals of European ancestry, the clinical interpretation of genomic variants in individuals from diverse ethnic backgrounds remains a major diagnostic challenge. Here, we investigated the genetic cause of a complex neurodevelopmental phenotype in two Palestinian siblings.
Reham Khalaf‐Nazzal, Imad Dweikat, Nishanka Ubeyratna, James Fasham, Maysa Alawneh, Joseph Leslie, Mosab Maree, Adam Gunning, Deyala Z. Zayed, Nikol Voutsina, Lucy McGavin, Reem Sawafta, Martina Owens, Wisam Baker, Peter Turnpenny, Fida’ Al‐Hijawi, Emma L. Baple, Andrew H. Crosby, Lettie E. Rawlins   +18 more
wiley   +1 more source

Institution Building in Myanmar: The Establishment of Regional and State Assemblies [PDF]

, 2015
published_or_final_versio
Aung, MH, Holliday, IM, Joelene, C
core   +1 more source

Familial Dysautonomia: Mechanisms and Models

Genetics and Molecular Biology
Hereditary Sensory and Autonomic Neuropathies (HSANs) compose a heterogeneous group of genetic disorders characterized by sensory and autonomic dysfunctions.
Paula Dietrich, Ioannis Dragatsis
doaj   +3 more sources