-
1
-
-
0003073254
-
The hyperphenylalaminaemias
-
In, Lloyd JK, Scriver CR, editors., London, Buttenvorth
-
Smith I. The hyperphenylalaminaemias. In: Lloyd JK, Scriver CR, editors. Genetic and Metabolic Disease. London : Buttenvorth, 1985: 166-209.
-
(1985)
Genetic and Metabolic Disease
, pp. 166-209
-
-
Smith, I.1
-
2
-
-
0025914001
-
Review of neonatal screening programme for phenylketonuria
-
Smith I, Cook B, Beasley M. Review of neonatal screening programme for phenylketonuria. BMJ 1991; 303: 333-335.
-
(1991)
BMJ
, vol.303
, pp. 333-335
-
-
Smith, I.1
Cook, B.2
Beasley, M.3
-
3
-
-
0019156116
-
Maternal phenylketonuria and hyperphenylalaninaemia: An international survey of the outcome of untreated and treated pregnancies
-
Lenke RR, Levy HL. Maternal phenylketonuria and hyperphenylalaninaemia: an international survey of the outcome of untreated and treated pregnancies. N Engl J Med 1980; 303: 1202-1208.
-
(1980)
N Engl J Med
, vol.303
, pp. 1202-1208
-
-
Lenke, R.R.1
Levy, H.L.2
-
4
-
-
0021040495
-
Effects of untreated maternal phenylketonuria and hyperphenylalaninaemia in the fetus
-
Levy HL, Waisbren SE. Effects of untreated maternal phenylketonuria and hyperphenylalaninaemia in the fetus. N Engl J Med 1983; 309: 1269-1273.
-
(1983)
N Engl J Med
, vol.309
, pp. 1269-1273
-
-
Levy, H.L.1
Waisbren, S.E.2
-
5
-
-
0023640629
-
Timing of strict diet in relation to fetal damage in maternal phenylketonuria: An international collaborative study by the MRCDHSS Phenylketonuria Register
-
Drogari E, Beasley M, Smith I, Lloyd JK. Timing of strict diet in relation to fetal damage in maternal phenylketonuria: an international collaborative study by the MRCDHSS Phenylketonuria Register. Lancet 1987; 2: 927-930.
-
(1987)
Lancet
, vol.2
, pp. 927-930
-
-
Drogari, E.1
Beasley, M.2
Smith, I.3
Lloyd, J.K.4
-
6
-
-
0025989477
-
Pregnancy in phenylketonuria: Dietary treatment aimed at normalising maternal plasma phenylalanine concentration
-
Thompson GN, Francis DE, Kirby DM, Compton R. Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentration. Arch Dis Child 1991; 66: 1346-1349.
-
(1991)
Arch Dis Child
, vol.66
, pp. 1346-1349
-
-
Thompson, G.N.1
Francis, D.E.2
Kirby, D.M.3
Compton, R.4
-
7
-
-
0027442890
-
The North American Collaboration study of maternal phenylketonuria
-
Koch R, Levy HL, Matalon R. Bobbye R et al. The North American Collaboration study of maternal phenylketonuria. Am J Dis Child 1993; 147: 1224-1230.
-
(1993)
Am J Dis Child
, vol.147
, pp. 1224-1230
-
-
Koch, R.1
Levy, H.L.2
Matalon, R.3
Bobbye, R.4
-
8
-
-
0026607030
-
Maternal phenylke tonuria collaberative study, obstetric aspects and outcome: The first 6 years
-
Plat LD, Koch R, Azen C, Hanley WB et al. Maternal phenylke tonuria collaberative study, obstetric aspects and outcome: the first 6 years. Am J Obstet Gynecol 1992; 166: 1150-1160.
-
(1992)
Am J Obstet Gynecol
, vol.166
, pp. 1150-1160
-
-
Plat, L.D.1
Koch, R.2
Azen, C.3
Hanley, W.B.4
-
9
-
-
0013977629
-
Standards from birth to maturity for height, weight, height velocity and weight velocity: British children, 1965
-
Tanner JM, Whitehouse RH, Takaishi M. Standards from birth to maturity for height, weight, height velocity and weight velocity: British children, 1965. Arch Dis Child 1966; 41: 613-635.
-
(1966)
Arch Dis Child
, vol.41
, pp. 613-635
-
-
Tanner, J.M.1
Whitehouse, R.H.2
Takaishi, M.3
-
10
-
-
0020389542
-
Projections in frequency of mental retardation from phenylketonuria
-
Kirkman HN. Projections in frequency of mental retardation from phenylketonuria. Appl Res Ment Retard 1982; 3: 319-321.
-
(1982)
Appl Res Ment Retard
, vol.3
, pp. 319-321
-
-
Kirkman, H.N.1
-
11
-
-
0027397393
-
Phenylketonuria due to phenylalanine hydroxylase deficiency, an unfolding story
-
MRC Working Party on Phenylketonuria. Phenylketonuria due to phenylalanine hydroxylase deficiency, an unfolding story. BMJ 1993; 306: 115-119.
-
(1993)
BMJ
, vol.306
, pp. 115-119
-
-
|