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Jump to: C | F | H | K | L | M | O | R | W
Number of items: 13.

C

COLLINGE, J; BROWN, J; HARDY, J; MULLAN, M; ROSSOR, MN; BAKER, H; CROW, TJ; (1992) INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .2. CLINICAL AND PATHOLOGICAL FEATURES. BRAIN , 115 687 - 710.

F

Fidani, L; Rooke, K; Chartier-Harlin, MC; Hughes, D; Tanzi, R; Mullan, M; Roques, P; (1992) Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile. Hum Mol Genet , 1 (3) pp. 165-168.

H

Hamvas, RMJ; Zinn, A; Keer, JT; Fisher, EMC; Beer-Romero, P; Brown, SDM; Page, D; (1992) Rps4 maps near the inactivation center on the mouse X chromosome. Genomics , 12 pp. 363-367.

K

KAPOOR, R; REVESZ, T; POWELL, M; (1992) SOLITARY CERVICAL LYMPHOMA PRESENTING AS A NEUROFIBROMA. BRIT J NEUROSURG , 6 (6) 583 - 586.

L

LANTOS, PL; LUTHERT, PJ; HANGER, D; ANDERTON, BH; MULLAN, M; ROSSOR, M; (1992) FAMILIAL ALZHEIMERS-DISEASE WITH THE AMYLOID PRECURSOR PROTEIN POSITION-717 MUTATION AND SPORADIC ALZHEIMERS-DISEASE HAVE THE SAME CYTOSKELETAL PATHOLOGY. NEUROSCI LETT , 137 (2) 221 - 224.

LANTOS, PL; MCGILL, IS; JANOTA, I; DOEY, LJ; COLLINGE, J; BRUCE, MT; WHATLEY, SA; (1992) PRION PROTEIN IMMUNOCYTOCHEMISTRY HELPS TO ESTABLISH THE TRUE INCIDENCE OF PRION DISEASES. NEUROSCI LETT , 147 (1) 67 - 71.

M

MULLAN, M; HOULDEN, H; WINDELSPECHT, M; FIDANI, L; LOMBARDI, C; DIAZ, P; ROSSOR, M; (1992) A LOCUS FOR FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASE ON THE LONG ARM OF CHROMOSOME 14, PROXIMAL TO THE ALPHA-1-ANTICHYMOTRYPSIN GENE. NAT GENET , 2 (4) 340 - 342.

O

O'Sullivan, F; Rossor, M; Elston, JS; (1992) Amaurosis fugax in young people. Br J Ophthalmol , 76 (11) pp. 660-662.

R

ROSSOR, M; (1992) ALZHEIMERS-DISEASE. POSTGRADUATE MEDICAL JOURNAL , 68 (801) pp. 528-532.

ROSSOR, MN; (1992) FAMILIAL ALZHEIMERS-DISEASE. BAILLIERE CLIN NEUR , 1 (3) 517 - 534.

ROSSOR, MN; KENNEDY, AM; NEWMAN, SK; (1992) HETEROGENEITY IN FAMILIAL ALZHEIMERS-DISEASE. In: Boller, F and Forette, F and Khachaturian, Z and Poncet, M and Christen, Y, (eds.) HETEROGENEITY OF ALZHEIMERS DISEASE. (pp. 81 - 87). SPRINGER-VERLAG BERLIN

Rossor, MN; (1992) Unusual dementias. Introduction. Baillieres Clin Neurol , 1 (3) pp. 477-483.

W

Warren, JD; Miles, TS; Trker, KS; (1992) Properties of synaptic noise in tonically active human motoneurons. J Electromyogr Kinesiol , 2 (4) pp. 189-202. 10.1016/1050-6411(92)90023-C.

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