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The Australasian Journal of Dermatology
|
January 27, 2005
Blau syndrome presenting with ichthyosis
Grant Masel, Anne Halbert
Pediatric Dermatology
|
November 17, 2017
Fibroadipose vascular anomaly treated with sirolimus: Successful outcome in two patients
Jonathan Erickson, William McAuliffe, Lewis Blennerhassett, et al.
Pediatric Dermatology
|
September 19, 2019
Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumab
Cathryn Poulton, Dylan Gration, Kevin Murray, et al.
The Australasian Journal of Dermatology
|
August 13, 2011
Dermatology outpatient population profiling: indigenous and non-indigenous dermatoepidemiology
Christopher Heyes, Jonathan Chan, Anne Halbert, et al.
Pediatric Dermatology
|
April 24, 2020
Cutaneous manifestations of congenital malignant rhabdoid tumor: Unusual papillomatous plaques and other skin presentations
Minnelly Luu, Anne Halbert, Albert Yan, et al.
The Australasian Journal of Dermatology
|
September 4, 2022
Discoid (nummular) eczema in the paediatric setting - An Australian/New Zealand narrative
Seamus McWhirter, Rachael Foster, Anne Halbert, et al.
The Australasian Journal of Dermatology
|
March 11, 2015
Adverse effects of topical corticosteroids in paediatric eczema: Australasian consensus statement
Emma Mooney, Marius Rademaker, Rebecca Dailey, et al.
The Australasian Journal of Dermatology
|
March 3, 2017
Consensus statement for the treatment of infantile haemangiomas with propranolol
Sarah L Smithson, Marius Rademaker, Susan Adams, et al.
Journal of Paediatrics and Child Health
|
June 1, 2026
Development of Multidisciplinary Consensus-Informed Guidance for the Management of Paediatric Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Among Clinicians From Australasian Tertiary Referral Hospitals
Patrick David Mahar, Thomas Lee, David Orchard, et al.
Nature Genetics
|
April 2, 2013
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome
Laura M McDonell, Ghayda M Mirzaa, Diana Alcantara, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
The Australasian Journal of Dermatology
|
January 27, 2005
Blau syndrome presenting with ichthyosis
Grant Masel, Anne Halbert
Pediatric Dermatology
|
November 17, 2017
Fibroadipose vascular anomaly treated with sirolimus: Successful outcome in two patients
Jonathan Erickson, William McAuliffe, Lewis Blennerhassett, et al.
Pediatric Dermatology
|
September 19, 2019
Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumab
Cathryn Poulton, Dylan Gration, Kevin Murray, et al.
The Australasian Journal of Dermatology
|
August 13, 2011
Dermatology outpatient population profiling: indigenous and non-indigenous dermatoepidemiology
Christopher Heyes, Jonathan Chan, Anne Halbert, et al.
Pediatric Dermatology
|
April 24, 2020
Cutaneous manifestations of congenital malignant rhabdoid tumor: Unusual papillomatous plaques and other skin presentations
Minnelly Luu, Anne Halbert, Albert Yan, et al.
The Australasian Journal of Dermatology
|
September 4, 2022
Discoid (nummular) eczema in the paediatric setting - An Australian/New Zealand narrative
Seamus McWhirter, Rachael Foster, Anne Halbert, et al.
The Australasian Journal of Dermatology
|
March 11, 2015
Adverse effects of topical corticosteroids in paediatric eczema: Australasian consensus statement
Emma Mooney, Marius Rademaker, Rebecca Dailey, et al.
The Australasian Journal of Dermatology
|
March 3, 2017
Consensus statement for the treatment of infantile haemangiomas with propranolol
Sarah L Smithson, Marius Rademaker, Susan Adams, et al.
Journal of Paediatrics and Child Health
|
June 1, 2026
Development of Multidisciplinary Consensus-Informed Guidance for the Management of Paediatric Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Among Clinicians From Australasian Tertiary Referral Hospitals
Patrick David Mahar, Thomas Lee, David Orchard, et al.
Nature Genetics
|
April 2, 2013
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome
Laura M McDonell, Ghayda M Mirzaa, Diana Alcantara, et al.
Page
of 1