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The Journal of Pediatrics
|
September 5, 2017
Prenatal Risk Factors for PHACE Syndrome: A Study Using the PHACE Syndrome International Clinical Registry and Genetic Repository
Joy Wan, Jack Steiner, Eulalia Baselga, 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 American Journal of Cardiology
|
October 2, 2013
Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry)
Michelle L Bayer, Peter C Frommelt, Francine Blei, 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.
Circulation
|
July 9, 2017
Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling
Mustapha Amyere, Nicole Revencu, Raphaël Helaers, et al.
The New England Journal of Medicine
|
February 19, 2015
A randomized, controlled trial of oral propranolol in infantile hemangioma
Christine Léauté-Labrèze, Peter Hoeger, Juliette Mazereeuw-Hautier, et al.
Human Mutation
|
September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation
Nicole Revencu, Laurence M Boon, Antonella Mendola, et al.
Science Immunology
|
June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
Vivien Béziat, Juan Li, Jian-Xin Lin, et al.
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of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
The Journal of Pediatrics
|
September 5, 2017
Prenatal Risk Factors for PHACE Syndrome: A Study Using the PHACE Syndrome International Clinical Registry and Genetic Repository
Joy Wan, Jack Steiner, Eulalia Baselga, 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 American Journal of Cardiology
|
October 2, 2013
Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry)
Michelle L Bayer, Peter C Frommelt, Francine Blei, 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.
Circulation
|
July 9, 2017
Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling
Mustapha Amyere, Nicole Revencu, Raphaël Helaers, et al.
The New England Journal of Medicine
|
February 19, 2015
A randomized, controlled trial of oral propranolol in infantile hemangioma
Christine Léauté-Labrèze, Peter Hoeger, Juliette Mazereeuw-Hautier, et al.
Human Mutation
|
September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation
Nicole Revencu, Laurence M Boon, Antonella Mendola, et al.
Science Immunology
|
June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
Vivien Béziat, Juan Li, Jian-Xin Lin, et al.
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of 5