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Group by: Author | Type
Jump to: A | B | C | G | H | L | M | W
Number of items: 13.

A

ADLARD, P; YIYAN, Y; BUZI, F; JONES, J; PREECE, MA; (1986) PULSATILE PROLACTIN SECRETION IN HYPOTHALAMIC-PITUITARY DISORDERS. PEDIATR RES , 20 (11) 1188 - 1188.

B

BRIGGS, M; JACOBY, J; DAVIDOWITZ, J; MOORE, G; SCHACHAT, F; (1986) THE EXTRAOCULAR-MUSCLES EXPRESS AN UNUSUAL COMBINATION OF FAST AND SLOW TROPONIN-T SPECIES. BIOPHYSICAL JOURNAL , 49 (2) A252 - A252.

BROOK, CGD; HINDMARSH, PC; HEALY, MJR; (1986) A BETTER WAY TO DETECT GROWTH FAILURE. BRIT MED J , 293 (6556) 1186 - 1186.

BROOK, CGD; HINDMARSH, PC; SMITH, PJ; STANHOPE, R; (1986) CLINICAL-FEATURES AND INVESTIGATION OF GROWTH-HORMONE DEFICIENCY. CLIN ENDOCRINOL META , 15 (3) 479 - 493.

C

Clayton, PT; Smith, I; Harding, B; Hyland, K; Leonard, JV; Leeming, RJ; (1986) Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism. J Neurol Neurosurg Psychiatry , 49 (8) 920 - 927.

G

GREENE, S; REES, L; ADLARD, P; JONES, J; CHANTLER, C; PREECE, M; (1986) ABNORMAL OVERNIGHT HORMONE PROFILES IN ADOLESCENTS WITH RENAL-DISEASE RECEIVING LONG-TERM STEROID-THERAPY. PEDIATR RES , 20 (11) 1204 - 1204.

H

HINDMARSH, PC; BROOK, CGD; (1986) TESTS FOR GROWTH-HORMONE DEFICIENCY - REPLY. LANCET , 1 (8471) 48 - 48.

HINDMARSH, PC; STANHOPE, R; KENDALL, BE; BROOK, CGD; (1986) TALL STATURE - A CLINICAL, ENDOCRINOLOGIC AND RADIOLOGICAL STUDY. CLIN ENDOCRINOL , 25 (3) 223 - 231.

HINDMARSH, PC; STANHOPE, R; SMITH, PJ; PRINGLE, PJ; BROOK, CGD; (1986) REPRODUCIBILITY OF 24 HOUR GROWTH-HORMONE PROFILES IN CHILDREN. J ENDOCRINOL , 108 308 - 308.

L

Lawson, AM; Madigan, MJ; Shortland, D; Clayton, PT; (1986) Rapid diagnosis of Zellweger syndrome and infantile Refsum's disease by fast atom bombardment-mass spectrometry of urine bile salts. Clinica Chimica Acta , 161 (2) 221 - 231.

M

MOORE, G; ROSES, A; PERICAKVANCE, M; GARRETT, W; SCHACHAT, F; (1986) PROMISCUOUS EXPRESSION OF MYOSIN IN MYOTONIC-DYSTROPHY. MUSCLE & NERVE , 9 (4) 355 - 363. 10.1002/mus.880090413.

W

Wales, JKH; Walker, V; Moore, IE; Clayton, PT; (1986) Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11. European Journal of Pediatrics , 145 (1-2) 141 - 143. 10.1007/BF00441878.

Walter, JH; Clayton, PT; Leonard, JV; (1986) 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency. J Inherit Metab Dis , 9 (3) 287 - 288.

This list was generated on Sun Jul 27 09:36:26 2014 BST.