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Items: 33

1.

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.

Hui L, Poulton A, Kluckow E, Lindquist A, Hutchinson B, Pertile MD, Bonacquisto L, Gugasyan L, Kulkarni A, Harraway J, Howden A, McCoy R, Costa FDS, Menezes M, Palma-Dias R, Nisbet D, Martin N, Bethune M, Poulakis Z, Halliday J.

Hum Reprod. 2020 Mar 27;35(3):694-704. doi: 10.1093/humrep/dez286.

PMID:
32207823
2.

Youths with a non-binary gender identity: a review of their sociodemographic and clinical profile.

Chew D, Tollit MA, Poulakis Z, Zwickl S, Cheung AS, Pang KC.

Lancet Child Adolesc Health. 2020 Apr;4(4):322-330. doi: 10.1016/S2352-4642(19)30403-1. Epub 2020 Jan 21. Review.

PMID:
31978373
3.

Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

Downie L, Halliday J, Burt R, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter MF, Saunders K, Rose E, Lewis S, Jarmolowicz A, Phelan D, Rehm HL; Melbourne Genomics Health Alliance, Amor DJ.

Eur J Hum Genet. 2019 Dec 12. doi: 10.1038/s41431-019-0553-8. [Epub ahead of print]

PMID:
31827275
4.

Abstracts of the 29th World Congress on Ultrasound in Obstetrics and Gynecology, 12-16 October 2019, Berlin, Germany.

Hui L, Lindquist A, Poulton A, Kluckow E, Hutchinson B, Bonacquisto L, Pertile MD, Gugasyan L, Kulkarni A, Harraway J, Howden A, McCoy R, da Silva Costa F, Palma-Dias R, Nisbet D, Martin N, Behune M, Poulakis Z, Halliday J.

Ultrasound Obstet Gynecol. 2019 Oct;54 Suppl 1:1-462. doi: 10.1002/uog.20426. No abstract available.

PMID:
31799705
5.

Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.

Kluckow E, Halliday J, Poulton A, Lindquist A, Hutchinson B, Bethune M, Bonacquisto L, Da Silva Costa F, Gugasyan L, Harraway J, Howden A, Kulkarni A, Martin N, McCoy R, Menezes M, Nisbet D, Palma-Dias R, Pertile MD, Poulakis Z, Hui L.

Prenat Diagn. 2019 Dec;39(13):1254-1261. doi: 10.1002/pd.5577. Epub 2019 Nov 6.

PMID:
31691307
6.

State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study.

Hui L, Lindquist A, Poulton A, Kluckow E, Hutchinson B, Pertile MD, Bonacquisto L, Gugasyan L, Kulkarni A, Harraway J, Howden A, McCoy R, da Silva Costa F, Menezes M, Palma-Dias R, Nisbet D, Martin N, Bethune M, Poulakis Z, Halliday J.

Ultrasound Obstet Gynecol. 2019 Oct 17. doi: 10.1002/uog.21899. [Epub ahead of print]

PMID:
31625225
7.

Data Resource Profile: The Victorian Childhood Hearing Impairment Longitudinal Databank (VicCHILD).

Sung V, Smith L, Poulakis Z, Burt RA, Carew P, Tobin S, Wake M.

Int J Epidemiol. 2019 Oct 1;48(5):1409-1410h. doi: 10.1093/ije/dyz168. No abstract available.

PMID:
31411681
8.

Transgender adolescents and legal reform: How improved access to healthcare was achieved through medical, legal and community collaboration.

Telfer M, Kelly F, Feldman D, Stone G, Robertson R, Poulakis Z.

J Paediatr Child Health. 2018 Oct;54(10):1096-1099. doi: 10.1111/jpc.14124.

PMID:
30294980
9.

Consider the costs of aiding mild hearing loss in the absence of clear benefits: Response to McCreery and colleagues.

Carew P, Mensah FK, Rance G, Flynn T, Poulakis Z, Wake M.

Child Care Health Dev. 2018 Nov;44(6):928-929. doi: 10.1111/cch.12601. No abstract available.

PMID:
30281850
10.

A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.

Downie L, Halliday JL, Burt RA, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter M, Saunders K, Rose E, Rehm HL, Amor DJ.

BMJ Paediatr Open. 2017 Sep 14;1(1):e000119. doi: 10.1136/bmjpo-2017-000119. eCollection 2017.

11.

Mild-moderate congenital hearing loss: secular trends in outcomes across four systems of detection.

Carew P, Mensah FK, Rance G, Flynn T, Poulakis Z, Wake M.

Child Care Health Dev. 2018 Jan;44(1):71-82. doi: 10.1111/cch.12477. Epub 2017 Jun 14.

PMID:
28612343
12.

Population Outcomes of Three Approaches to Detection of Congenital Hearing Loss.

Wake M, Ching TY, Wirth K, Poulakis Z, Mensah FK, Gold L, King A, Bryson HE, Reilly S, Rickards F.

Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-1722. Epub 2015 Dec 24.

13.

The cost-effectiveness of universal newborn screening for bilateral permanent congenital hearing impairment: systematic review.

Colgan S, Gold L, Wirth K, Ching T, Poulakis Z, Rickards F, Wake M.

Acad Pediatr. 2012 May-Jun;12(3):171-80. doi: 10.1016/j.acap.2012.02.002. Review.

14.

Slight-mild sensorineural hearing loss in children: audiometric, clinical, and risk factor profiles.

Cone BK, Wake M, Tobin S, Poulakis Z, Rickards FW.

Ear Hear. 2010 Apr;31(2):202-12. doi: 10.1097/AUD.0b013e3181c62263.

PMID:
20054279
15.

Children subjected to cardiac surgery for congenital heart disease. Part 2 - parental emotional experiences.

Menahem S, Poulakis Z, Prior M.

Interact Cardiovasc Thorac Surg. 2008 Aug;7(4):605-8. doi: 10.1510/icvts.2007.171066. Epub 2008 May 19.

PMID:
18490367
16.

Children subjected to cardiac surgery for congenital heart disease. Part 1 - emotional and psychological outcomes.

Menahem S, Poulakis Z, Prior M.

Interact Cardiovasc Thorac Surg. 2008 Aug;7(4):600-4. doi: 10.1510/icvts.2007.171058. Epub 2008 May 19.

PMID:
18490364
17.

Slight/mild sensorineural hearing loss in children.

Wake M, Tobin S, Cone-Wesson B, Dahl HH, Gillam L, McCormick L, Poulakis Z, Rickards FW, Saunders K, Ukoumunne OC, Williams J.

Pediatrics. 2006 Nov;118(5):1842-51.

PMID:
17079553
19.

The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children.

Dahl HH, Tobin SE, Poulakis Z, Rickards FW, Xu X, Gillam L, Williams J, Saunders K, Cone-Wesson B, Wake M.

J Med Genet. 2006 Nov;43(11):850-5. Epub 2006 Jul 13.

20.

Prevalence, stability, and outcomes of cry-fuss and sleep problems in the first 2 years of life: prospective community-based study.

Wake M, Morton-Allen E, Poulakis Z, Hiscock H, Gallagher S, Oberklaid F.

Pediatrics. 2006 Mar;117(3):836-42.

PMID:
16510665
21.

The distraction test: the last word?

Russ SA, Poulakis Z, Wake M, Barker M, Rickards F, Jarman FC, Saunders K, Edwards G, Symons L, Oberklaid F.

J Paediatr Child Health. 2005 Apr;41(4):197-200.

PMID:
15813874
22.

Hearing impairment: a population study of age at diagnosis, severity, and language outcomes at 7-8 years.

Wake M, Poulakis Z, Hughes EK, Carey-Sargeant C, Rickards FW.

Arch Dis Child. 2005 Mar;90(3):238-44.

23.

Parent-reported health-related quality of life in children with congenital hearing loss: a population study.

Wake M, Hughes EK, Collins CM, Poulakis Z.

Ambul Pediatr. 2004 Sep-Oct;4(5):411-7.

PMID:
15369416
24.

Qualitative analysis of parents' experience with early detection of hearing loss.

Russ SA, Kuo AA, Poulakis Z, Barker M, Rickards F, Saunders K, Jarman FC, Wake M, Oberklaid F.

Arch Dis Child. 2004 Apr;89(4):353-8.

25.

Outcomes of children with mild-profound congenital hearing loss at 7 to 8 years: a population study.

Wake M, Hughes EK, Poulakis Z, Collins C, Rickards FW.

Ear Hear. 2004 Feb;25(1):1-8.

PMID:
14770013
26.

Slight and mild hearing loss in primary school children.

Wake M, Poulakis Z.

J Paediatr Child Health. 2004 Jan-Feb;40(1-2):11-3.

PMID:
14717996
27.

Epidemiology of congenital hearing loss in Victoria, Australia.

Russ SA, Poulakis Z, Barker M, Wake M, Rickards F, Saunders K, Oberklaid F.

Int J Audiol. 2003 Oct;42(7):385-90.

PMID:
14582634
28.

Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutations.

Dahl HH, Wake M, Sarant J, Poulakis Z, Siemering K, Blamey P.

Audiol Neurootol. 2003 Sep-Oct;8(5):263-8.

PMID:
12904681
29.

Six month impact of false positives in an Australian infant hearing screening programme.

Poulakis Z, Barker M, Wake M.

Arch Dis Child. 2003 Jan;88(1):20-4.

30.

Six year effectiveness of a population based two tier infant hearing screening programme.

Russ SA, Rickards F, Poulakis Z, Barker M, Saunders K, Wake M.

Arch Dis Child. 2002 Apr;86(4):245-50.

31.

Clinical markers of serious illness in young infants: a multicentre follow-up study.

Hewson P, Poulakis Z, Jarman F, Kerr J, McMaster D, Goodge J, Silk G.

J Paediatr Child Health. 2000 Jun;36(3):221-5.

PMID:
10849220
32.

Late diagnosis of congenital sensorineural hearing impairment: why are detection methods failing?

Robertson C, Aldridge S, Jarman F, Saunders K, Poulakis Z, Oberklaid F.

Arch Dis Child. 1995 Jan;72(1):11-5.

33.

Phosphate compounds in erythrocytes and plasma in Duchenne muscular dystrophy.

KaloFoutis A, Poulakis Z.

Clin Chem. 1984 Jun;30(6):1101-2. No abstract available.

PMID:
6723020

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