Results 181 to 190 of about 9,576 (247)

Guillain-Barré Syndrome With Asymmetrical Weakness in a Patient With Charcot-Marie-Tooth Disease Type 1A. [PDF]

Cureus
Ahmed K, Elachola M, Alsararatee H, Pugh N.   +3 more
europepmc   +1 more source

Unraveling the Overlapping Spectrum of Hereditary Neuropathies: Clinical and Genetic Insights From the UAE. [PDF]

Cureus
Jumani A, Rashwan G, Ibrahim H, Eissa H, Abouelnaga ME, Alzaabi A, Elbashari M.   +6 more
europepmc   +1 more source

Severe axonal neuropathy is a late manifestation of SPG11 [PDF]

core   +1 more source

Clinical and genetic analysis of a family with transthyretin amyloid polyneuropathy caused by a TTR Lys55Asn mutation. [PDF]

Orphanet J Rare Dis
Qian N, Wei T, Qian Y, Yang W, Han H, Chen H, Li J.   +6 more
europepmc   +1 more source

Hereditary Polyneuropathies in the Era of Precision Medicine: Genetic Complexity and Emerging Strategies. [PDF]

Genes (Basel)
Chrysostomaki M, Chatzi D, Kyriakoudi SA, Meditskou S, Manthou ME, Gargani S, Theotokis P, Dermitzakis I.   +7 more
europepmc   +1 more source

The effect of high-dose long-term therapy of intravenous immunoglobulins in autoimmune autonomic and sensory small fiber neuropathy: a retrospective open-label controlled study. [PDF]

Sci Rep
Novak P, Witte A, Marciano SP, Felsenstein D, Ngo L.   +4 more
europepmc   +1 more source

Charcot-Marie-Tooth Disease With Persistent Perioperative Hypotension due to Autonomic Dysfunction: A Case Report. [PDF]

Case Rep Anesthesiol
Singh K, Lawrence AM.
europepmc   +1 more source

Polyneuropathy in hereditary and wildtype transthyretin amyloidosis, comparison of key clinical features and red flags. [PDF]

Sci Rep
Siemer JM, Grote-Levi L, Hänselmann A, Sassmann ML, Nay S, Ratuszny D, Körner S, Seeliger T, Hümmert MW, Dohrn MF, Huss A, Tumani H, Gödecke V, Heuser M, Bauersachs J, Bavendiek U, Skripuletz T, Gingele S.   +17 more
europepmc   +1 more source

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia. [PDF]

BMC Med Genomics
Yuan X, Zhang S, Tang Y.
europepmc   +1 more source

The Vagal Link: Autonomic Nervous System Dysfunction in Cardiac Amyloidosis. [PDF]

J Clin Med
Barocelli F, Canu E, Pasini N, Allegri I, D'Orsi A, Bettella A, Crocamo A, Gurgoglione FL, Torlai Triglia L, Russo F, Guidorossi A, Notarangelo MF, Gaibazzi N, Ruffini L, Niccoli G.   +14 more
europepmc   +1 more source