Detalhe da pesquisa
1.
Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects.
Prenat Diagn
; 42(7): 862-872, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35441720
2.
Stillbirth rate in singleton pregnancies: a 20-year retrospective study from a public obstetric unit in Hong Kong.
Hong Kong Med J
; 28(4): 285-293, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35058373
3.
Perinatal mortality rate in multiple pregnancies: a 20-year retrospective study from a tertiary obstetric unit in Hong Kong.
Hong Kong Med J
; 2022 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36059150
4.
Neonatal mortality in singleton pregnancies: a 20-year retrospective study from a tertiary perinatal unit in Hong Kong.
Hong Kong Med J
; 28(6): 430-437, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36442841
5.
Transperineal ultrasound assessment of fetal head elevation by maneuvers used for managing umbilical cord prolapse.
Ultrasound Obstet Gynecol
; 58(4): 603-608, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33219729
6.
Outcome of radiofrequency ablation for selective fetal reduction before vs at or after 16 gestational weeks in complicated monochorionic pregnancy.
Ultrasound Obstet Gynecol
; 58(2): 214-220, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32730679
7.
Prenatal diagnosis of ascending aortic aneurysm associated with sternal cleft.
Ultrasound Obstet Gynecol
; 59(2): 267-268, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33998075
8.
Triplet pregnancy with fetal reduction: experience in Hong Kong.
Hong Kong Med J
; 23(4): 326-32, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28642442
9.
Bronchopulmonary sequestration successfully treated with prenatal radiofrequency ablation of feeding artery.
Ultrasound Obstet Gynecol
; 58(2): 325-327, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32898279
10.
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
Nat Genet
; 13(2): 214-8, 1996 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-8640229
11.
Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
J Clin Invest
; 92(2): 612-6, 1993 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8102379
12.
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.
J Clin Invest
; 95(3): 1174-82, 1995 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-7883966
13.
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.
J Clin Invest
; 89(3): 892-8, 1992 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-1541680
14.
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
J Clin Invest
; 86(3): 909-16, 1990 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1975598
15.
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.
J Clin Invest
; 88(1): 76-81, 1991 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-2056132
16.
Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase.
Gene
; 88(2): 293-6, 1990 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-2347496
17.
IV pentamidine for Pneumocystis jiroveci pneumonia prophylaxis in pediatric allogeneic stem cell transplant patients.
Bone Marrow Transplant
; 51(10): 1394-1396, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27214074
18.
Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.
Semin Perinatol
; 14(5): 351-67, 1990 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-2287951
19.
Age-dependent pharmacokinetic profile of single daily dose i.v. busulfan in children undergoing reduced-intensity conditioning stem cell transplant.
Bone Marrow Transplant
; 44(3): 145-56, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19182832
20.
Red blood cell membrane disorders.
Br J Haematol
; 104(1): 2-13, 1999 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-10027705