P. Benson

发表

Elevated erythrocyte 2,3-diphosphoglycerate concentration in primary trisomic Down's syndrome.

E. Nelson, P. Benson, 1972, Archives of disease in childhood.

Response of infants to pertussis vaccine at one week and to poliomyelitis, diphtheria, and tetanus vaccine at six months.

P. Benson, A. Beale, N. Butler, 1962, Lancet.

Phototherapy for Pruritus in Chronic Cholestasis of Childhood

P. Benson, D. Vulliamy, J. Taubman, 1982 .

Congenital hemihypertrophy and malignancy.

P. Benson, D. Vulliamy, J. Taubman, 1963, Lancet.

Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.

C. Rodeck, P. Benson, A. Fensom, 1979, British medical journal.

GM1-generalized gangliosidosis variant with cardiomegaly

P. Benson, T. Mann, S. Brown, 1976, Postgraduate medical journal.

Ulcerative colitis in childhood. A study of its natural history.

P. Benson, J. Platt, B. Schlesinger, 1960, The Quarterly journal of medicine.

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems.

P. Benson, M. Seller, P. Polani, 1979, Journal of medical genetics.

Cardiomegaly in a Newborn Due to Placental Chorioangioma

P. Benson, M. Joseph, 1961, British medical journal.

FLUORIMETRIC ASSAY FOR PRENATAL DETECTION OF HURLER AND SCHEIE HOMOZYGOTES OR HETEROZYGOTES

P. Benson, J. Stirling, A. Fensom, 1978, The Lancet.

PRENATAL DIAGNOSIS OF TWO HURLER FETUSES USING AN IMPROVED ASSAY FOR METHYLUMBELLIFERYL-α-L-IDURONEDASE

P. Benson, J. Stirling, A. Fensom, 1979, The Lancet.

PRENATAL DIAGNOSIS FOR METABOLIC DISORDER

P. Benson, P. Polani, A. Fensom, 1979, The Lancet.

Diminished activity of platelet monoamine oxidase in Down's syndrome.

J. Southgate, P. Benson, 1971, American journal of human genetics.

Changes in the Circulation at Birth

P. Benson, 1961, Cerebral palsy bulletin.

Effect of aluminium phosphate on antibody response to killed poliomyelitis vaccne.

P. Benson, A. Beale, N. Butler, 1962, Lancet.

In vivo effect of adenosine 3',5'-monophosphate on Ehrlich ascites tumour cells.

P. Benson, M. Seller, 1973, Archives of disease in childhood.

In vivo effect of adenosine 3',5'-monophosphate on Ehrlich ascites tumour cells.

P. Benson, M. Seller, 1973, European journal of cancer.

RAISED INTRACRANIAL PRESSURE ASSOCIATED WITH TRIAMCINOLONE

P. Benson, P. Pharoah, 1960 .

Screening and management of potentially treatable genetic metabolic disorders

P. Benson, 1984 .

An outbreak of exfoliative dermatitis of the newborn (Ritter's disease) due to Staphylococcus aureus, phage-type 55/71.

P. Benson, J. Rippey, G. Rankin, 1962, Lancet.

Progressive mental regression in siblings with Morquio disease Type B (mucopolysaccharidosis IV B)

P. Benson, M. Jackson, S. Skinner, 1987, Clinical genetics.

Vaccination of Infants with Living Attenuated Measles Vaccine (Edmonston Strain) with and without Gamma-globulin

G. Knight, P. Benson, N. Butler, 1964, British medical journal.

Biochemical abnormalities in chromosome anomalies.

P. Benson, 1971, Lancet.

PRENATAL DIAGNOSIS OF FARBER'S DISEASE

H. Moser, A. Moser, P. Benson, 1979, The Lancet.

Massive Foetal Haemorrhage into Maternal Circulation as a Complication of Choriocarcinoma

P. Benson, K. Goldsmith, G. Rankin, 1962, British medical journal.

A Case of Calcification of the Basal Ganglia with Osteoporosis and Other Abnormalities

P. Benson, 1959, Archives of disease in childhood.

Fibroblast phosphodiesterase deficiency in Niemann-Pick disease.

P. Benson, A. Fensom, L. Jacobs, 1977, Biochemical and biophysical research communications.

Prenatal Diagnosis of Galactosaemia

P. Benson, A. Fensom, S. Blunt, 1974, British medical journal.

Prenatal exclusion of Hurler's disease by leucocyte α‐L‐iduronidase assay

P. Benson, C. H. Rodeck, A. H. Fensom, 1983 .

Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia.

P. Benson, A. Fensom, 1975, Clinica chimica acta; international journal of clinical chemistry.

The biochemistry of development

P. Benson, 1971 .

Maple syrup urine disease with increased intracranial pressure.

P. Benson, V. D. Der Kaloustian, M. Mikati, 1982, American journal of diseases of children.

Prenatal diagnosis of galactosaemia in six pregnancies' possible complications with rare alleles of the galactose 1‐phosphate uridyl transferase locus

E. Christensen, P. Benson, N. Brandt, 1979, Clinical genetics.

TRANSIENT AND INTERMITTENT SYSTOLIC MURMURS IN NEWBORN INFANTS

P. Benson, J. Smellie, R. Bonham-Carter, 1961 .

INTELLECTUAL IMPAIRMENT IN CONGENITAL LARYNGEAL STRIDOR.

P. Benson, R. Benians, R. Spector, 1964, Guy's Hospital reports.

Lymphangiography and Chromosome Studies in Females with Lymphoedema and Possible Ovarian Dysgenesis

P. Benson, P. Polani, M. Gough, 1965, Archives of disease in childhood.

The Prognosis of Subdural Effusions Complicating Pyogenic Meningitis

W. Nyhan, P. Benson, H. Shimizu, 1960 .

DETECTION OF CYSTIC FIBROSIS WITH PLASMA HYDROLASES

P. Benson, A. Fensom, A. Harris, 1979, The Lancet.

Congenital Dysphagia Resulting from Dysfunction of the Pharyngeal Musculature A Clinical and Radiological Study

G. Ardran, P. Benson, N. Butler, 1965, Developmental medicine and child neurology.

Total surgical correction of Fallot's tetralogy in the first year of life.

D. Ross, P. Benson, M. Joseph, 1962, Lancet.

CONGENITAL MITRAL STENOSIS

D. Ross, P. Benson, C. Baker, 1962, British heart journal.

A reliable qualitative urine coproporphyrin test for lead intoxication in young children.

P. Benson, J. Chisolm, J. Chisolm, 1960, The Journal of pediatrics.

Recent advances in the prenatal diagnosis of the mucopolysaccharidoses

P. Benson, A. Fensom, 1994, Prenatal diagnosis.

Correct prenatal diagnosis of a hurler fetus where amniotic fluid cell cultures were of maternal origin

P. Benson, A. D. Patrick, A. H. Fensom, 1981, Prenatal diagnosis.

GENE DOSAGE EFFECT IN TRISOMY 21

P. Benson, 1975, The Lancet.

Metabolic Disease in Childhood

P. Benson, 1979 .

The Effect of Dextran Infusions on Glycosaminoglycan Excretion in the Sanfilippo Syndrome

P. Benson, M. Dean, H. Muir, 1975, Developmental medicine and child neurology.

Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidase.

P. Benson, J. Stirling, A. Fensom, 1979, Lancet.

Diminished activity of platelet monoamine oxidase in Down's syndrome.

J. Southgate, P. Benson, 1970, Archives of Disease in Childhood.

Prenatal exclusion of homocystinuria (cystathionine β‐synthase deficiency) by assay of phytohaemagglutinin‐stimulated fetal lymphocytes

C. Rodeck, P. Benson, A. Fensom, 1983, Prenatal diagnosis.

Chromosome anomalies in primary lymphoedema.

P. Benson, M. Gough, A. I. Taylor, 1967, Lancet.

Genetic Metabolic Diseases. Early Diagnosis and Prenatal Analysis

P. Benson, 1981 .

Amniotic-cell galactokinase activity: stimulation by galactose.

P. Benson, S. Blunt, S. Brown, 1973, Lancet.

Fibroblast α-galactosidase a activity for identification of Fabry's disease heterozygotes

P. Benson, A. Fensom, L. Jacobs, 1979, Journal of Inherited Metabolic Disease.

Rickets in Immigrant Children in London

A. Nicolaides, P. Benson, C. Stroud, 1963, British medical journal.

Transient Unilateral External Rectus Muscle Palsy in Newborn Infants

P. Benson, 1962, British medical journal.

Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria.

C. Rodeck, P. Benson, R. Chalmers, 1984, Journal of inherited metabolic disease.

Further Observations on Vaccination in Infancy with Oral Poliomyelitis Vaccine and Diphtheria, Tetanus, Pertussis Vaccine

G. Knight, P. Benson, N. Butler, 1964, British medical journal.

Poliomyelitis antibody titres in children and effect of live and inactivated poliovaccine.

C. Oddy, P. Benson, R. Yetts, 1969, Lancet.

Cellular Organelles and Membranes in Mental Retardation

P. Benson, Multiple Handicap, 1972, Psychological Medicine.

Letter: Schilder's disease: cholesterol metabolism in cultured fibroblasts.

P. Benson, A. Fensom, J. Wilson, 1976, Archives of disease in childhood.

Blood Brain Barrier

P. Benson, M. Joseph, 1961, Cerebral palsy bulletin.

Transient Dysphagia Due to Muscular Inco-Ordination

P. Benson, R. Keith, 1962, Proceedings of the Royal Society of Medicine.

CONGENITAL MITRAL STENOSIS

D. Ross, P. Benson, C. Baker, 1962, British heart journal.

A mild form of mucolipidosis type III in four Baluch siblings

P. Benson, A. Hasilik, A. Fensom, 1993, Clinical genetics.

Corneal clouding in GM1-generalized gangliosidosis.

P. Benson, A. Fensom, A. Babarik, 1976, The British journal of ophthalmology.