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Genes & Genomics
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March 9, 2021
Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families
Obaid Ur Rahman, Jeena Kim, Caroline Mahon, et al.
The Australasian Journal of Dermatology
|
June 10, 2025
A Retrospective Observational Study of the Incidence and Associated Risk Factors of Skin Cancers in Renal Transplant Recipients in Canterbury, New Zealand
Julia Xiaoyu Zhu, Eve Mallon, Caroline Mahon, et al.
Pediatric Dermatology
|
July 19, 2019
Panniculitis in a 3-year-old child with Fanconi anemia-associated bone marrow hypoplasia heralds transformation to acute myeloid leukemia
Lucy Webber, Michelle Cummins, Rebecca Mann, et al.
The Australasian Journal of Dermatology
|
June 4, 2019
Aerosolised deodorant-induced bullous dermatitis artefacta: A clinicopathological correlation
Caroline Mahon, Lucy Webber, Nicholas Bisson, et al.
Pediatric Pulmonology
|
July 7, 2021
Surveillance of pediatric parapneumonic effusion/empyema in New Zealand
Katherine Rix-Trott, Catherine A Byrnes, Catherine A Gilchrist, et al.
The Australasian Journal of Dermatology
|
July 22, 2021
A baseline patch test series for New Zealand
Adrian J Seine, Elizabeth Ann Baird, Lydia Chan, et al.
The British Journal of Dermatology
|
July 18, 2023
A novel rapamycin cream formulation improves facial angiofibromas associated with tuberous sclerosis complex: a double-blind randomized placebo-controlled trial
Phillip Aitken, Ioana Stanescu, Laura Boddington, et al.
The Journal of Clinical Investigation
|
November 2, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
The Journal of Clinical Investigation
|
February 21, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Genes & Genomics
|
March 9, 2021
Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families
Obaid Ur Rahman, Jeena Kim, Caroline Mahon, et al.
The Australasian Journal of Dermatology
|
June 10, 2025
A Retrospective Observational Study of the Incidence and Associated Risk Factors of Skin Cancers in Renal Transplant Recipients in Canterbury, New Zealand
Julia Xiaoyu Zhu, Eve Mallon, Caroline Mahon, et al.
Pediatric Dermatology
|
July 19, 2019
Panniculitis in a 3-year-old child with Fanconi anemia-associated bone marrow hypoplasia heralds transformation to acute myeloid leukemia
Lucy Webber, Michelle Cummins, Rebecca Mann, et al.
The Australasian Journal of Dermatology
|
June 4, 2019
Aerosolised deodorant-induced bullous dermatitis artefacta: A clinicopathological correlation
Caroline Mahon, Lucy Webber, Nicholas Bisson, et al.
Pediatric Pulmonology
|
July 7, 2021
Surveillance of pediatric parapneumonic effusion/empyema in New Zealand
Katherine Rix-Trott, Catherine A Byrnes, Catherine A Gilchrist, et al.
The Australasian Journal of Dermatology
|
July 22, 2021
A baseline patch test series for New Zealand
Adrian J Seine, Elizabeth Ann Baird, Lydia Chan, et al.
The British Journal of Dermatology
|
July 18, 2023
A novel rapamycin cream formulation improves facial angiofibromas associated with tuberous sclerosis complex: a double-blind randomized placebo-controlled trial
Phillip Aitken, Ioana Stanescu, Laura Boddington, et al.
The Journal of Clinical Investigation
|
November 2, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
The Journal of Clinical Investigation
|
February 21, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
Page
of 2