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Orbital Fractures and Air Travel

The Journal of craniofacial surgery, 2021-06, Vol.32 (4), p.1625-1627

2021

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Sterilization of bedside 3D-printed devices for use in the operating room

Annals of 3D printed medicine, 2022-03, Vol.5, p.100045, Article 100045

2022

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Warfarin-induced skin necrosis progressing to calciphylaxis

Journal of plastic, reconstructive & aesthetic surgery, 2014-10, Vol.67 (10), p.e244-e246

2014

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Prevention of surgical fires in facial plastic surgery

Australasian journal of plastic surgery, 2019-09, Vol.2 (2), p.40-49

2019

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Anterolateral thigh flap fascia lata suspension in oral floor reconstruction

The Laryngoscope, 2011-03, Vol.121 (3), p.555-557

2011

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Predicting the prognosis of oral squamous cell carcinoma after first recurrence

Archives of otolaryngology--head & neck surgery, 2010-12, Vol.136 (12), p.1235

2010

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The management of hereditary melanoma, FAMMM syndrome and germline CDKN2A mutations: a narrative review

Australasian journal of plastic surgery, 2022-09, Vol.5 (2), p.12-22

2022

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Number of nodal metastases and prognosis in metastatic cutaneous squamous cell carcinoma of the head and neck

ANZ journal of surgery, 2019-07, Vol.89 (7-8), p.863-867

2019

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A Cross Sectional, Mixed-Method Cohort Study Evaluating the Implementation of Leading Better Value Care Initiatives

Journal of service science and management, 2021, Vol.14 (2), p.228-240

2021

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Z-Plasty Modification of Ulnar-Based Fasciocutaneous Flap for Closure of the Radial Forearm Flap Donor Defect

Annals of plastic surgery, 2010, Vol.64 (1), p.22-23

2010

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Magnetic resonance imaging: is a single scan ever enough for the diagnosis of acoustic neuroma?

Journal of laryngology and otology, 2006-12, Vol.120 (12), p.1061-1063

2006

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Warfarin-induced skin necrosis progressing to calciphylaxis

Journal of plastic, reconstructive & aesthetic surgery : JPRAS, 2014, Vol.67 (10), p.e244-e246

2014

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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

American journal of human genetics, 2015-12, Vol.97 (6), p.886-893

2015

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ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regions

Human molecular genetics, 2015-04, Vol.24 (7), p.1824-1835

2015

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Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery

American journal of human genetics, 2022-11, Vol.109 (11), p.1947-1959

2022

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Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada

Genetics in medicine, 2022-01, Vol.24 (1), p.100-108

2022

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IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA

Movement disorders, 2024-09

2024

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Quality indicators for Palliative Day Services: A modified Delphi study

Palliative medicine, 2019-02, Vol.33 (2), p.197-205

2019

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220 Cochrane review of interval brain imaging in adults with cerebral glioma

Journal of neurology, neurosurgery and psychiatry, 2022-06, Vol.93 (6), p.A76-A76

2022

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Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ: Report of seven new subjects and review of the literature

Journal of inherited metabolic disease, 2020-11, Vol.43 (6), p.1321-1332

2020

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Combined conservative and orthotic management of acute ruptures of the Achilles tendon

Journal of bone and joint surgery. American volume, 2004-06, Vol.86 (6), p.1198-1202

2004

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Interval brain imaging for adults with cerebral glioma

Cochrane database of systematic reviews, 2019-12, Vol.12 (12), p.CD013137-CD013137

2019

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Intraoperative imaging technology to maximise extent of resection for glioma: a network meta-analysis

Cochrane database of systematic reviews, 2021-01, Vol.1 (1), p.CD013630

2021

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The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability

American journal of human genetics, 2022-10, Vol.109 (10), p.1923-1931

2022

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Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability

Human molecular genetics, 2015-11, Vol.24 (22), p.6293-6300

2015

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Orbital Fractures and Air Travel

Sterilization of bedside 3D-printed devices for use in the operating room

Warfarin-induced skin necrosis progressing to calciphylaxis

Prevention of surgical fires in facial plastic surgery

Anterolateral thigh flap fascia lata suspension in oral floor reconstruction

Predicting the prognosis of oral squamous cell carcinoma after first recurrence

The management of hereditary melanoma, FAMMM syndrome and germline CDKN2A mutations: a narrative review

Number of nodal metastases and prognosis in metastatic cutaneous squamous cell carcinoma of the head and neck

A Cross Sectional, Mixed-Method Cohort Study Evaluating the Implementation of Leading Better Value Care Initiatives

Z-Plasty Modification of Ulnar-Based Fasciocutaneous Flap for Closure of the Radial Forearm Flap Donor Defect

Magnetic resonance imaging: is a single scan ever enough for the diagnosis of acoustic neuroma?

Warfarin-induced skin necrosis progressing to calciphylaxis

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regions

Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery

Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada

IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA

Quality indicators for Palliative Day Services: A modified Delphi study

220 Cochrane review of interval brain imaging in adults with cerebral glioma

Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ: Report of seven new subjects and review of the literature

Combined conservative and orthotic management of acute ruptures of the Achilles tendon

Interval brain imaging for adults with cerebral glioma

Intraoperative imaging technology to maximise extent of resection for glioma: a network meta-analysis

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability

Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability

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