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A Mutation Outside the Dimerization Domain Causing Atypical STING-Associated Vasculopathy With Onset in Infancy

Frontiers in immunology, 2018-07, Vol.9, p.1535-1535

2018

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Chicken skin gelatin films with tapioca starch

Food bioscience, 2020-06, Vol.35, p.100589, Article 100589

2020

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The Role of Sonic Hedgehog in Human Holoprosencephaly and Short-Rib Polydactyly Syndromes

International journal of molecular sciences, 2021-09, Vol.22 (18), p.9854

2021

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Vitamin A status in human fetuses with congenital diaphragmatic hernia: (Author reply to comment by Rocke AW and Clugston RD)

Early human development, 2018-01, Vol.116, p.94-94

2018

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Lung and liver growth and retinoic acid status in human fetuses with congenital diaphragmatic hernia

Early human development, 2018-01, Vol.116, p.17-23

2018

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Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome

Birth defects research. A Clinical and molecular teratology, 2016-07, Vol.106 (7), p.549-562

2016

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Paediatric Laryngeal Synovial Sarcoma: Dilemmas and Decision-Making

Case reports in otolaryngology, 2024-04, Vol.2024, p.7574240-5

2024

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Intramural implantation within adenomyosis proceeding to live birth of viable infant

Pathology, 2024-02, Vol.56, p.S40

2024

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The development of hepatic stellate cells in normal and abnormal human fetuses – an immunohistochemical study

Physiological reports, 2015-08, Vol.3 (8), p.e12504-n/a

2015

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Origin of stellate cells from submesothelial cells in a developing human liver

Liver international, 2008-11, Vol.28 (10), p.1437-1445

2008

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Case Report: Fetal Bilateral Diaphragmatic Agenesis, Ectopic Liver and Abnormal Pancreas

Fetal and pediatric pathology, 2015-08, Vol.34 (4), p.216-222

2015

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Challenges, experiences, and potential supports for East and Southeast Asian mothers in the workforce: a systematic review

BMC women's health, 2024-07, Vol.24 (1), p.1-16, Article 422

2024

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Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations

Birth defects research. A Clinical and molecular teratology, 2012-02, Vol.94 (2), p.116-122

2012

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Prognostic Significance of Vascular Endothelial Growth Factor in Squamous Cell Carcinomas of the Tonsil in Relation to Human Papillomavirus Status and Epidermal Growth Factor Receptor

Annals of surgical oncology, 2009-10, Vol.16 (10), p.2908-2917

2009

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Lack of cilia and differentiation defects in the liver of human foetuses with the Meckel syndrome

Liver international, 2008-03, Vol.28 (3), p.377-384

2008

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Possible Role of WT1 in a Human Fetus with Evolving Bronchial Atresia, Pulmonary Malformation and Renal Agenesis

Pediatric and developmental pathology, 2012-01, Vol.15 (1), p.39-44

2012

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Synovial sarcoma of the neck: A malignant mimic of a common benign cyst

Pathology, 2018-02, Vol.50, p.S82-S82

2018

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Antenatal gastrointestinal anomalies in neonates subsequently found to have alveolar capillary dysplasia

Clinical case reports, 2017-05, Vol.5 (5), p.559-566

2017

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Large proximal intertwin vascular anastomoses as a rare cause of twin anaemia-polycythaemia sequence (TAPS): case report

Pathology, 2023-02, Vol.55, p.S43-S43

2023

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Insulin-like Growth Factor-binding Protein-3 in Osteosarcomas and Normal Bone Tissues

Anticancer research, 2009-07, Vol.29 (7), p.2579-2587

2009

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A rare case of a rapidly expanding high flow vascular anomaly

Pathology, 2019-02, Vol.51, p.S104-S105

2019

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Cavernous hemangioma in median nerve in the cubital fossa: a rare cause of a median nerve lesion

Pathology, 2019-02, Vol.51, p.S105-S105

2019

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N-CAM and keratins 7 and 20 in the ductal plate malformation of the Meckel-Gruber syndrome

Pathology, 2006-08, Vol.38 (4), p.374-376

2006

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Mixed large cell neuroendocrine carcinoma and high grade serous carcinoma of the ovary: a histopathological case report

Pathology, 2023-02, Vol.55, p.S55-S55

2023

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An Audit of Atypical Thyroid FNA Using The Bethesda System for Reporting Thyroid Cytology (TBSRTC) in Regional NSW, Australia

Journal of the American Society of Cytopathology JASC, 2013-10, Vol.2 (1), p.S47-S47

2013

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A Mutation Outside the Dimerization Domain Causing Atypical STING-Associated Vasculopathy With Onset in Infancy

Chicken skin gelatin films with tapioca starch

The Role of Sonic Hedgehog in Human Holoprosencephaly and Short-Rib Polydactyly Syndromes

Vitamin A status in human fetuses with congenital diaphragmatic hernia: (Author reply to comment by Rocke AW and Clugston RD)

Lung and liver growth and retinoic acid status in human fetuses with congenital diaphragmatic hernia

Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome

Paediatric Laryngeal Synovial Sarcoma: Dilemmas and Decision-Making

Intramural implantation within adenomyosis proceeding to live birth of viable infant

The development of hepatic stellate cells in normal and abnormal human fetuses – an immunohistochemical study

Origin of stellate cells from submesothelial cells in a developing human liver

Case Report: Fetal Bilateral Diaphragmatic Agenesis, Ectopic Liver and Abnormal Pancreas

Challenges, experiences, and potential supports for East and Southeast Asian mothers in the workforce: a systematic review

Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations

Prognostic Significance of Vascular Endothelial Growth Factor in Squamous Cell Carcinomas of the Tonsil in Relation to Human Papillomavirus Status and Epidermal Growth Factor Receptor

Lack of cilia and differentiation defects in the liver of human foetuses with the Meckel syndrome

Possible Role of WT1 in a Human Fetus with Evolving Bronchial Atresia, Pulmonary Malformation and Renal Agenesis

Synovial sarcoma of the neck: A malignant mimic of a common benign cyst

Antenatal gastrointestinal anomalies in neonates subsequently found to have alveolar capillary dysplasia

Large proximal intertwin vascular anastomoses as a rare cause of twin anaemia-polycythaemia sequence (TAPS): case report

Insulin-like Growth Factor-binding Protein-3 in Osteosarcomas and Normal Bone Tissues

A rare case of a rapidly expanding high flow vascular anomaly

Cavernous hemangioma in median nerve in the cubital fossa: a rare cause of a median nerve lesion

N-CAM and keratins 7 and 20 in the ductal plate malformation of the Meckel-Gruber syndrome

Mixed large cell neuroendocrine carcinoma and high grade serous carcinoma of the ovary: a histopathological case report

An Audit of Atypical Thyroid FNA Using The Bethesda System for Reporting Thyroid Cytology (TBSRTC) in Regional NSW, Australia

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