Results 181 to 190 of about 10,587 (266)

The NGF^R100W Mutation Specifically Impairs Nociception without Affecting Cognitive Performance in a Mouse Model of Hereditary Sensory and Autonomic Neuropathy Type V. [PDF]

J Neurosci, 2019
Testa G, Mainardi M, Morelli C, Olimpico F, Pancrazi L, Petrella C, Severini C, Florio R, Malerba F, Stefanov A, Strettoi E, Brandi R, Arisi I, Heppenstall P, Costa M, Capsoni S, Cattaneo A.   +16 more
europepmc   +1 more source

Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1C. [PDF]

Cold Spring Harb Mol Case Stud, 2017
Auranen M, Toppila J, Suriyanarayanan S, Lone MA, Paetau A, Tyynismaa H, Hornemann T, Ylikallio E.   +7 more
europepmc   +1 more source

Multiple symmetric lipomatosis [PDF]

, 1994
Bischof, F., Eckert, P., Klopstock, Thomas, Kottlors, M., Naumann, M., Reichmann, Heinz, Reiners, K., Schalke, B., Seibel, P., Toyka, K.   +9 more
core   +1 more source

Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease [PDF]

core   +1 more source

Hereditary sensory and autonomic neuropathy type IV.

Indian pediatrics, 2006
Sunil, Karande, Nitin, Satam
openaire   +1 more source

Oral manifestations and prosthetic rehabilitation in hereditary sensory and autonomic neuropathy (HSAN)type IV: a case report. [PDF]

J Istanb Univ Fac Dent, 2016
Ofluoglu D, Altin N, Yaman E, Tuna İnce EB, Aytepe Z, Tanyeri H.   +5 more
europepmc   +1 more source

Retrospective Review of 56 Patients with Sensory Ganglionopathy. [PDF]

Noro Psikiyatr Ars
Uzunçakmak-Uyanık H, Temuçin ÇM, Tan E, Göçmen R, Yıldız FG.   +4 more
europepmc   +1 more source

新規プリオン遺伝子変異「コドン178の2塩基欠失」により引き起こされる「PrP systemic deposition病」の臨床及び病理学的な特徴 [PDF]

, 2017
Matsuzono, Kosuke
core  

The Role of Skin Innervation for Assessment of Neurological Involvement in Disorders: A Review. [PDF]

Brain Sci
Furia A, Ragucci C, Liguori R, Rizzo G, Vacchiano V, Giannoccaro MP, Donadio VA.   +6 more
europepmc   +1 more source

p.Asp58Val Hereditary Transthyretin Amyloidosis: A Case Report and Literature Review. [PDF]

Cureus
Ramnarain J, Hosking P, Gibbs S.
europepmc   +1 more source