Results 251 to 260 of about 78,837 (263)

Association of co-existing vitamin B6 and B12 deficiency with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes (POEMS) syndrome: a case report. [PDF]

BMC Neurol
Hu S, Brown-Kunin S, Martin P, Wang Y.
europepmc   +1 more source

Reassessing the Role of the Neurofilament Light Chain in Guillain-Barre Syndrome: Issues in Diagnosis and Subgroup Classification. [PDF]

Eur J Neurol
Seok HY, Eun MY.
europepmc   +1 more source

Effect of Transcutaneous Application of Carbon Dioxide on Wound Healing, Wound Recurrence Rate and Diabetic Polyneuropathy in Patients with Neuropathic, Ischemic and Neuroischemic Diabetes-Related Foot Ulcers. [PDF]

Life (Basel)
Bulum T, Poljičanin T, Badanjak A, Držič J, Metelko Ž.   +4 more
europepmc   +1 more source

Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22. [PDF]

Neurogenetics
Kawai H, Nishida Y, Kanda T, Yokota T.
europepmc   +1 more source

Gait changes with aging: an early warning sign for underlying pathology. [PDF]

J Neurol
Nonnekes J, Post E, Imbalzano G, Bloem BR.   +3 more
europepmc   +1 more source

Eculizumab as a Disease-Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Case Report. [PDF]

J Peripher Nerv Syst
Schilke ED, Cereda D, Fusco ML, Stanzani L, Marzorati L, Ripolone M, Bertolasi L, Frigo M, Molteni F, Farina N, Ferrarese C, Cavaletti G, Balducci C.   +12 more
europepmc   +1 more source

A Case of Guillain-Barré Syndrome Possibly Associated With COVID-19 Infection. [PDF]

Cureus
Giannas R, Klironomou L, Skafida E.
europepmc   +1 more source

Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy: A Randomized Clinical Trial With Open-Label Extension.

JAMA Neurol
Adams D, Wixner J, Polydefkis M, Berk JL, Conceição IM, Dispenzieri A, Peltier A, Ueda M, Bender S, Capocelli K, Jay PY, Yureneva E, Obici L, patisiran Global OLE study group.   +13 more
europepmc   +1 more source

A Rare Presentation of Patient With CIDP Found to Have Respiratory Failure and Encephalopathy. [PDF]

Case Rep Crit Care
Sheth P, Rodriguez Lopez A, Acharya S, Dunn B.   +3 more
europepmc   +1 more source

Expanding the Genetic and Clinical Spectrum of Hereditary Transthyretin Amyloidosis: The Glu61Ala Variant. [PDF]

J Pers Med
Messina C, Gulizia S, Scalia F, Borgione E, Cappello F, Brighina F, Di Stefano V.   +6 more
europepmc   +1 more source