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Albert C Yan

Showing results (121-130 of 135) with videos related to

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HPB : the Official Journal of the International Hepato Pancreato Biliary Association|July 19, 2018
Recurrent pyogenic cholangitis - an independent poor prognostic indicator for resectable intrahepatic cholangiocarcinoma: A propensity score matched analysisKa W Ma, Tan T Cheung, Wong H She, et al.
Clinical Pediatrics|May 23, 2014
Retrospective analysis of beta-blocker instituted for treatment of hemangiomas (RABBIT study)Derek H Chu, Leslie Castelo-Soccio, Joy Wan, et al.
JAMA Dermatology|January 30, 2020
Development and Initial Validation of a Multidimensional Acne Global Grading System Integrating Primary Lesions and Secondary ChangesElena Bernardis, Haochang Shou, John S Barbieri, et al.
Pediatric Dermatology|December 27, 2024
Infantile Hemangioma With Aggressive, Early-Onset Ulceration, and Kasabach-Merritt-Like Phenomenon in a NewbornCharles Y Huang, María Trinidad Hasbún, Robert F Duffy, et al.
Pediatric Dermatology|July 6, 2019
Pediatric leukemia cutis: A case seriesElena Corina Andriescu, Carrie C Coughlin, Carol E Cheng, et al.
Pediatric Dermatology|February 18, 2026
Leg Length Discrepancy in Patients With Lower Extremity Cutis Marmorata Telangiectatica Congenita: A Multicenter Retrospective StudyRacquel A Bitar, Sarah E Servattalab, Marilyn G Liang, et al.
Archives of Dermatology|December 21, 2005
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotypeAimee S Payne, Albert C Yan, Erum Ilyas, et al.
Journal of the American Academy of Dermatology|December 24, 2025
Cutaneous adverse events associated with MEK-inhibitors for the treatment of vascular anomalies: a dual-center retrospective studyIsabella R Plumptre, Racquel A Bitar, Pierre-Olivier Grenier, et al.
Orphanet Journal of Rare Diseases|January 25, 2012
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutationsElisa A Colombo, J Fernando Bazan, Gloria Negri, et al.
JAMA Dermatology|May 6, 2026
Pediatric Skin Disease Frequencies and Dermatology Use by Race and Ethnicity in US Children's HospitalsNicolas G Quan, Elizabeth Garcia-Creighton, Molly Thapar, et al.
Pageof 14

Showing results (121-130 of 135) with videos related to

Sort By:
Pageof 14
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|July 19, 2018
Recurrent pyogenic cholangitis - an independent poor prognostic indicator for resectable intrahepatic cholangiocarcinoma: A propensity score matched analysisKa W Ma, Tan T Cheung, Wong H She, et al.
Clinical Pediatrics|May 23, 2014
Retrospective analysis of beta-blocker instituted for treatment of hemangiomas (RABBIT study)Derek H Chu, Leslie Castelo-Soccio, Joy Wan, et al.
JAMA Dermatology|January 30, 2020
Development and Initial Validation of a Multidimensional Acne Global Grading System Integrating Primary Lesions and Secondary ChangesElena Bernardis, Haochang Shou, John S Barbieri, et al.
Pediatric Dermatology|December 27, 2024
Infantile Hemangioma With Aggressive, Early-Onset Ulceration, and Kasabach-Merritt-Like Phenomenon in a NewbornCharles Y Huang, María Trinidad Hasbún, Robert F Duffy, et al.
Pediatric Dermatology|July 6, 2019
Pediatric leukemia cutis: A case seriesElena Corina Andriescu, Carrie C Coughlin, Carol E Cheng, et al.
Pediatric Dermatology|February 18, 2026
Leg Length Discrepancy in Patients With Lower Extremity Cutis Marmorata Telangiectatica Congenita: A Multicenter Retrospective StudyRacquel A Bitar, Sarah E Servattalab, Marilyn G Liang, et al.
Archives of Dermatology|December 21, 2005
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotypeAimee S Payne, Albert C Yan, Erum Ilyas, et al.
Journal of the American Academy of Dermatology|December 24, 2025
Cutaneous adverse events associated with MEK-inhibitors for the treatment of vascular anomalies: a dual-center retrospective studyIsabella R Plumptre, Racquel A Bitar, Pierre-Olivier Grenier, et al.
Orphanet Journal of Rare Diseases|January 25, 2012
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutationsElisa A Colombo, J Fernando Bazan, Gloria Negri, et al.
JAMA Dermatology|May 6, 2026
Pediatric Skin Disease Frequencies and Dermatology Use by Race and Ethnicity in US Children's HospitalsNicolas G Quan, Elizabeth Garcia-Creighton, Molly Thapar, et al.
Pageof 14