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Items: 1 to 50 of 76

1.

Measuring the quality of life of the families of children with eczema in Hong Kong.

Cheng NS, Chau PCJ, Hon KLE, Choi KC, Kung JSC, Ng WG, Leung TF.

Asia Pac Allergy. 2019 Jul 17;9(3):e26. doi: 10.5415/apallergy.2019.9.e26. eCollection 2019 Jul.

2.

Testing an ectoin containing emollient for atopic dermatitis.

Hon KLE, Kung JSC, Ng WGG, Leung TF.

Curr Pediatr Rev. 2019 Apr 15. doi: 10.2174/1573396315666190415144244. [Epub ahead of print]

PMID:
30987568
3.

Chronic Urticaria: An Overview of Treatment and Recent Patents.

Hon KL, Leung AKC, Ng WGG, Loo SK.

Recent Pat Inflamm Allergy Drug Discov. 2019;13(1):27-37. doi: 10.2174/1872213X13666190328164931.

4.

Utility of the Pediatric Allergic Disease Quality of Life Questionnaire for childhood eczema.

Hon KL, Ng WGG, Kung JSC, Cheng NS, Ng DKK, Leung TF.

Br J Dermatol. 2019 Aug;181(2):290-295. doi: 10.1111/bjd.17710. Epub 2019 May 6.

PMID:
30706447
5.

Assessment of adherence to eczema treatment in Hong Kong children.

Cheng NS, Chau JPC, Hon KLE, Choi KC, Kung JSC, Ng WG, Leung TF.

J Dermatolog Treat. 2019 Dec;30(8):790-795. doi: 10.1080/09546634.2019.1573304. Epub 2019 Feb 12.

PMID:
30663920
6.

Pilot Studies on Two Complementary Bath Products for Atopic Dermatitis Children: Pine-Tar and Tea.

Hon KL, Ng WGG, Kung JSC, Leung PC, Leung TF.

Medicines (Basel). 2019 Jan 8;6(1). pii: E8. doi: 10.3390/medicines6010008.

7.

Neonatal epidermolysis bullosa: Lessons to learn about genetic counselling.

Chong SC, Hon KL, Yuen L, Choi CL, Ng WGG, Chiu T.

J Dermatolog Treat. 2018 Oct 3:1-14. doi: 10.1080/09546634.2018.1527999. [Epub ahead of print]

PMID:
30280950
8.

Confirming Distal Perfusion Catheter Position by Micro-bubbles in Patients on Peripheral Venoarterial Extracorporeal Membrane Oxygenation.

Au SY, Fong KM, Ng WG, Leung KA.

ASAIO J. 2019 Sep/Oct;65(7):753-755. doi: 10.1097/MAT.0000000000000868.

PMID:
30153197
9.

Emollient treatment of atopic dermatitis: latest evidence and clinical considerations.

Hon KL, Kung JSC, Ng WGG, Leung TF.

Drugs Context. 2018 Apr 17;7:212530. doi: 10.7573/dic.212530. eCollection 2018. Review.

10.

Are skin equipment for assessing childhood eczema any good?

Hon KL, Kung J, Ng WG, Tsang K, Cheng NS, Leung TF.

J Dermatolog Treat. 2018 Feb 20:1-15. doi: 10.1080/09546634.2018.1442551. [Epub ahead of print]

PMID:
29460656
11.

Two adult galactosaemia females with normal ovarian function and identical GALT mutations (Q188R/R333G).

Ng WG, Xu YK, Wong LJ, Kaufman FR, Buist NR, Donnell GN.

J Inherit Metab Dis. 2003;26(1):75-9.

PMID:
12872845
12.

Association of galactose-1-phosphate uridyltransferase activity and N314D genotype with the risk of ovarian cancer.

Goodman MT, Wu AH, Tung KH, McDuffie K, Cramer DW, Wilkens LR, Terada K, Reichardt JK, Ng WG.

Am J Epidemiol. 2002 Oct 15;156(8):693-701.

PMID:
12370157
13.

A case-control study of galactose consumption and metabolism in relation to ovarian cancer.

Cramer DW, Greenberg ER, Titus-Ernstoff L, Liberman RF, Welch WR, Li E, Ng WG.

Cancer Epidemiol Biomarkers Prev. 2000 Jan;9(1):95-101.

14.

Molecular and biochemical basis of galactosemia.

Wang BB, Xu YK, Ng WG, Wong LJ.

Mol Genet Metab. 1998 Apr;63(4):263-9.

PMID:
9635294
15.

Endometriosis associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT).

Cramer DW, Hornstein MD, Ng WG, Barbieri RL.

Mol Hum Reprod. 1996 Mar;2(3):149-52.

PMID:
9238674
16.

HPLC analysis of uridine diphosphate sugars: decreased concentrations of uridine diphosphate galactose in erythrocytes and cultured skin fibroblasts from classical galactosemia patients.

Xu YK, Kaufman FR, Donnell GN, Giudici T, Alfi O, Ng WG.

Clin Chim Acta. 1995 Aug 31;240(1):21-33. No abstract available.

PMID:
8582057
17.
18.

Biochemical and molecular studies of 132 patients with galactosemia.

Ng WG, Xu YK, Kaufman FR, Donnell GN, Wolff J, Allen RJ, Koritala S, Reichardt JK.

Hum Genet. 1994 Oct;94(4):359-63.

19.

Characteristics of women with a family history of ovarian cancer. I. Galactose consumption and metabolism.

Cramer DW, Muto MG, Reichardt JK, Xu H, Welch WR, Valles B, Ng WG.

Cancer. 1994 Aug 15;74(4):1309-17.

PMID:
8055453
20.

Correlation of cognitive, neurologic, and ovarian outcome with the Q188R mutation of the galactose-1-phosphate uridyltransferase gene.

Kaufman FR, Reichardt JK, Ng WG, Xu YK, Manis FR, McBride-Chang C, Wolff JA.

J Pediatr. 1994 Aug;125(2):225-7.

PMID:
8040766
21.

On the molecular nature of the Duarte variant of galactose-1-phosphate uridyl transferase (GALT).

Lin HC, Kirby LT, Ng WG, Reichardt JK.

Hum Genet. 1994 Feb;93(2):167-9.

PMID:
8112740
22.

Measurements of uridine diphosphate hexoses in galactosemia.

Ng WG, Xu YK, Kaufman FR, Donnell GN.

J Pediatr. 1993 Dec;123(6):1015-6. No abstract available.

PMID:
8229509
23.

Neurologic complications in galactosemia.

Koch TK, Schmidt KA, Wagstaff JE, Ng WG, Packman S.

Pediatr Neurol. 1992 May-Jun;8(3):217-20.

PMID:
1622520
24.

Galactose consumption and metabolism in relation to the risk of ovarian cancer.

Cramer DW, Harlow BL, Willett WC, Welch WR, Bell DA, Scully RE, Ng WG, Knapp RC.

Lancet. 1989 Jul 8;2(8654):66-71.

PMID:
2567871
25.

Milk produced by mothers with galactosemia.

Ng WG, Xu YK, Kaufman F, Donnell GN.

J Pediatr. 1989 Jul;115(1):166-7. No abstract available.

PMID:
2738786
26.

Galactose-1-phosphate uridyl transferase activity associated with age at menopause and reproductive history.

Cramer DW, Harlow BL, Barbieri RL, Ng WG.

Fertil Steril. 1989 Apr;51(4):609-15.

PMID:
2538369
27.

Galactose metabolism in human ovarian tissue.

Xu YK, Ng WG, Kaufman FR, Lobo RA, Donnell GN.

Pediatr Res. 1989 Feb;25(2):151-5. Erratum in: Pediatr Res 1990 Feb;27(2):117.

PMID:
2919130
28.

Gonadal function and ovarian galactose metabolism in classic galactosemia.

Kaufman FR, Xu YK, Ng WG, Silva PD, Lobo RA, Donnell GN.

Acta Endocrinol (Copenh). 1989 Feb;120(2):129-33.

PMID:
2492704
29.

Uridine nucleotide sugars in erythrocytes of patients with galactokinase deficiency.

Xu YK, Ng WG, Kaufman FR, Donnell GN.

J Inherit Metab Dis. 1989;12(4):445-50.

PMID:
2516175
30.

Deficit of uridine diphosphate galactose in galactosaemia.

Ng WG, Xu YK, Kaufman FR, Donnell GN.

J Inherit Metab Dis. 1989;12(3):257-66.

PMID:
2515367
31.

Correlation of ovarian function with galactose-1-phosphate uridyl transferase levels in galactosemia.

Kaufman FR, Xu YK, Ng WG, Donnell GN.

J Pediatr. 1988 May;112(5):754-6. No abstract available. Erratum in: J Pediatr 1989 Aug;115(2):329.

PMID:
2834527
32.
33.

Müllerian aplasia associated with maternal deficiency of galactose-1-phosphate uridyl transferase.

Cramer DW, Ravnikar VA, Craighill M, Ng WG, Goldstein DP, Reilly R.

Fertil Steril. 1987 Jun;47(6):930-4.

PMID:
3036608
34.

Transferase-deficiency galactosemia and the Duarte variant.

Ng WG, Lee JS, Donnell GN.

JAMA. 1987 Jan 9;257(2):187-8. No abstract available.

PMID:
3795401
35.

Methylmalonic and propionic acidemias: lipid profiles of normal and affected human skin fibroblasts incubated with [1-14C]propionate.

Giudici TA, Chen RG, Oizumi J, Shaw KN, Ng WG, Donnell GN.

Biochem Med Metab Biol. 1986 Jun;35(3):384-98.

PMID:
2872907
36.

Pyruvate carboxylase defect: metabolic studies on cultured skin fibroblasts.

Oizumi J, Ng WG, Donnell GN.

J Inherit Metab Dis. 1986;9(2):120-8.

PMID:
3091918
37.

False-positive amniotic fluid acetylcholinesterase results: the need for a multifacet approach to the prenatal diagnosis of neural tube defects.

Lee JE, Ng WG, Falk RE, Alfi O, Lopez L, Platt LD.

Obstet Gynecol. 1985 Sep;66(3 Suppl):22S-24S.

PMID:
2410841
38.

Beta-glucuronidase deficiency. A heterogeneous mucopolysaccharidosis.

Lee JE, Falk RE, Ng WG, Donnell GN.

Am J Dis Child. 1985 Jan;139(1):57-9.

PMID:
3155909
39.

Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.

Oizumi J, Ng WG, Koch R, Shaw KN, Sweetman L, Velazquez A, Donnell GN.

Clin Genet. 1984 Jun;25(6):538-42.

PMID:
6733950
40.

Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.

Oizumi J, Donnell GN, Ng WG, Mulivor RA, Greene AE, Coriell LL.

Cytogenet Cell Genet. 1984;38(1):80. No abstract available.

PMID:
6705569
41.

Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria.

Oizumi J, Shaw KN, Giudici TA, Carter M, Donnell GN, Ng WG.

J Inherit Metab Dis. 1983;6(3):89-94.

PMID:
6422151
42.

Polymorphism of erythrocyte galactose-1-phosphate uridyltransferase among Chinese.

Xu YK, Ng WG.

Hum Genet. 1983;63(3):280-2. No abstract available.

PMID:
6303942
43.

Prenatal diagnosis of pseudo arylsulphatase A deficiency.

Kihara H, Fluharty AL, Tsay KK, Bachman RP, Stephens JD, Ng WG.

Prenat Diagn. 1983 Jan;3(1):29-34.

PMID:
6133271
44.

False negative maternal serum alpha-fetoprotein determinations in myelodysplasia: the role of ultrasound.

Platt LD, Golde SH, Artal R, Frohlich G, Alfi OL, Ng WG.

Am J Obstet Gynecol. 1982 Oct 1;144(3):352-5. No abstract available.

PMID:
6181687
45.

Semi-micro techniques for the genotyping of galactokinase and galactose-1-phosphate uridyltransferase.

Lee JE, Ng WG.

Clin Chim Acta. 1982 Sep 30;124(3):351-6. No abstract available.

PMID:
6290108
46.

Presymptomatic diagnosis: metachromatic leukodystrophy or pseudo arylsulphatase A deficiency?

Kihara H, Fluharty AL, Ng WG, Leider W.

J Inherit Metab Dis. 1982;5(4):215-7.

PMID:
6133034
47.

Carrier detection of urea cycle disorders.

Ng WG, Oizumi J, Koch R, Shaw KN, McLaren J, Donnel GN, Carter M.

Pediatrics. 1981 Sep;68(3):448-52. No abstract available.

PMID:
7279481
48.

Propionate metabolism by cultured skin fibroblasts from normal individuals and patients with methylmalonicaciduria and propionicacidemia.

Oizumi J, Giudici TA, Ng WG, Shaw KN, Donnell GN.

Biochem Med. 1981 Aug;26(1):28-40. No abstract available.

PMID:
7295302
49.

Abnormal urinary oligosaccharide pattern in patients with glycogen storage disease, type III.

McLaren J, Ng WG, Roe T.

Clin Chem. 1980 Dec;26(13):1924-5. No abstract available.

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