Results 211 to 220 of about 35,863 (248)

IL-8 and IL-1β in the Cerebrospinal Fluid of Patient With Creutzfeldt-Jakob Disease: A Case Report. [PDF]

Clin Case Rep
GuoYan L, ShuQin Z, HuiYang Q, MengYing C, HongWei R, Hong S.   +5 more
europepmc   +1 more source

Sporadic Creutzfeldt-Jakob Disease Complicated by Intracerebral Hemorrhaging in the Early Stage of Onset. [PDF]

Intern Med
Fujita M, Nishijima H, Mikami Y, Suzuki C, Tomiyama M.   +4 more
europepmc   +1 more source

Cadaveric Human Growth Hormone-Associated Creutzfeldt-Jakob Disease with Long Latency Period, United States. [PDF]

Emerg Infect Dis
Ribeiro AS, Wolf AB, Leschek EW, Schonberger LB, Abrams JY, Maddox RA, Appleby BS, Glisic K, Carlson A, Matthews E.   +9 more
europepmc   +1 more source

Alien Limb Phenomenon and Ideomotor Apraxia as Early Indicators of Sporadic Creutzfeldt-Jakob Disease. [PDF]

Mov Disord Clin Pract
Lueg G, Kleffner I, Hobert MA.
europepmc   +1 more source

Rapid Neurological Decline due to Creutzfeldt-Jakob Disease. [PDF]

J Community Hosp Intern Med Perspect
Tesoro N, Blackwood D, Reif R, Miller S, Paudel K, Haas C.   +5 more
europepmc   +1 more source

A dividing cell model for stable propagation and curing of bona fide human sporadic Creutzfeldt-Jakob Disease prions

Nihat A, Arora P, Schmidt C, Rayner ML, Linehan J, Brandner S, Mead S, Collinge J, Jat PS.   +8 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Creutzfeldt-Jakob Disease

Neurologic Clinics, 1986
There has been significant advance in our understanding of CJD and similar spongiform encephalopathies in recent years. The range in clinical expression of the disease is better appreciated, and the existence of "atypical" cases of CJD is increasingly recognized.
Z, Davanipour, M, Alter, E, Sobel
openaire   +2 more sources