Detalhe da pesquisa
1.
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease.
Nat Immunol
; 23(1): 75-85, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34937930
2.
Biallelic TLR4 deficiency in humans.
J Allergy Clin Immunol
; 151(3): 783-790.e5, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36462956
3.
Pediatric Cervicofacial Actinomycosis: Lessons From a Craniofacial Unit.
J Craniofac Surg
; 30(8): 2432-2438, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31306379
4.
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.
Am J Hum Genet
; 93(1): 6-18, 2013 Jul 11.
Artigo
Inglês
| MEDLINE | ID: mdl-23746549
5.
Haemophilus influenzae: a potent perinatal pathogen disproportionately isolated from Indigenous women and their neonates.
Aust N Z J Obstet Gynaecol
; 56(1): 75-81, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26503452
6.
Risk of cancer among children with birth defects: a novel approach.
Birth Defects Res A Clin Mol Teratol
; 103(4): 284-91, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25808250
7.
Connective tissue growth factor is expressed in bone marrow stromal cells and promotes interleukin-7-dependent B lymphopoiesis.
Haematologica
; 99(7): 1149-56, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24727816
8.
Solitary, multifocal and generalized myofibromas: clinicopathological and immunohistochemical features of 114 cases.
Histopathology
; 60(6B): E1-11, 2012 May.
Artigo
Inglês
| MEDLINE | ID: mdl-22486319
9.
Fetal akinesia: review of the genetics of the neuromuscular causes.
J Med Genet
; 48(12): 793-801, 2011 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21984750
10.
Fetal oromandibular limb hypogenesis syndrome following uterine curettage in early pregnancy.
Birth Defects Res A Clin Mol Teratol
; 91(4): 226-9, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21462298
11.
Human AGR2 Deficiency Causes Mucus Barrier Dysfunction and Infantile Inflammatory Bowel Disease.
Cell Mol Gastroenterol Hepatol
; 12(5): 1809-1830, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34237462
12.
Caudal dysgenesis and sirenomelia-single centre experience suggests common pathogenic basis.
Am J Med Genet A
; 152A(10): 2578-87, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20734338
13.
Infection and fetal loss in the mid-second trimester of pregnancy.
Aust N Z J Obstet Gynaecol
; 50(3): 221-5, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20618237
14.
Frequency and timing of loss of imprinting at 11p13 and 11p15 in Wilms' tumor development.
Mol Cancer Res
; 6(7): 1114-23, 2008 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-18644976
15.
Function of caspase-14 in trophoblast differentiation.
Reprod Biol Endocrinol
; 7: 98, 2009 Sep 14.
Artigo
Inglês
| MEDLINE | ID: mdl-19747408
16.
Fetal growth and the risk of childhood CNS tumors and lymphomas in Western Australia.
Int J Cancer
; 123(2): 436-443, 2008 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18412242
17.
Placental characteristics and birthweight.
Paediatr Perinat Epidemiol
; 22(3): 229-39, 2008 May.
Artigo
Inglês
| MEDLINE | ID: mdl-18426518
18.
Renal tumours of childhood: an update.
Pathology
; 40(2): 217-27, 2008 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-18203043
19.
The Possible Role of Placental Morphometry in the Detection of Fetal Growth Restriction.
Front Physiol
; 9: 1884, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-30670983
20.
Methods to decrease variability in histological scoring in placentas from a cohort of preterm infants.
BMJ Open
; 7(3): e013877, 2017 03 31.
Artigo
Inglês
| MEDLINE | ID: mdl-28363925