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Case Reports in Dermatology
|
June 28, 2021
Diffuse Facial Hyperpigmentation as a Presenting Sign of Lupus Erythematosus: Three Cases and Review of the Literature
Shir Azrielant, Eran Ellenbogen, Alon Peled, et al.
The British Journal of Dermatology
|
January 7, 2022
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-α and interleukin-12/23 blockade
Liat Samuelov, Ofer Sarig, Kiril Malovitski, et al.
Pediatric Dermatology
|
May 17, 2018
Risk factors for ocular complications in periocular infantile hemangiomas
Liat Samuelov, Michael Kinori, Karen Rychlik, et al.
Pediatric Dermatology
|
December 28, 2024
Beyond Classification: A Unique Case of Self-Resolving Cutaneous Mucinosis Associated With Streptococcal Infection in a Child
Ari Safir, Moran Furman, Andrea Gat, et al.
The Journal of Dermatology
|
July 28, 2023
Intralesional human papillomavirus vaccine for the treatment of recalcitrant cutaneous warts
Efrat Bar-Ilan, Jonathan Bar, Avital Baniel, et al.
The Journal of Pediatrics
|
October 2, 2018
Ocular Complications in PHACE Syndrome: A True Association or a Coincidence?
Liat Samuelov, Michael Kinori, Anthony J Mancini, et al.
Fertility and Sterility
|
July 4, 2012
An embryo cleavage pattern based on the relative blastomere size as a function of cell number for predicting implantation outcome
Roee Sela, Liat Samuelov, Benny Almog, et al.
Experimental Dermatology
|
April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneity
Shahar Taiber, Liat Samuelov, Janan Mohamad, et al.
Experimental Dermatology
|
March 3, 2012
Calcitonin gene-related peptide (CGRP) may award relative protection from interferon-γ-induced collapse of human hair follicle immune privilege
Michael Kinori, Marta Bertolini, Wolfgang Funk, et al.
The British Journal of Dermatology
|
July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes
Janan Mohamad, Ofer Sarig, Paula Beattie, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 61) with videos related to
Sort By:
Page
of 7
Case Reports in Dermatology
|
June 28, 2021
Diffuse Facial Hyperpigmentation as a Presenting Sign of Lupus Erythematosus: Three Cases and Review of the Literature
Shir Azrielant, Eran Ellenbogen, Alon Peled, et al.
The British Journal of Dermatology
|
January 7, 2022
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-α and interleukin-12/23 blockade
Liat Samuelov, Ofer Sarig, Kiril Malovitski, et al.
Pediatric Dermatology
|
May 17, 2018
Risk factors for ocular complications in periocular infantile hemangiomas
Liat Samuelov, Michael Kinori, Karen Rychlik, et al.
Pediatric Dermatology
|
December 28, 2024
Beyond Classification: A Unique Case of Self-Resolving Cutaneous Mucinosis Associated With Streptococcal Infection in a Child
Ari Safir, Moran Furman, Andrea Gat, et al.
The Journal of Dermatology
|
July 28, 2023
Intralesional human papillomavirus vaccine for the treatment of recalcitrant cutaneous warts
Efrat Bar-Ilan, Jonathan Bar, Avital Baniel, et al.
The Journal of Pediatrics
|
October 2, 2018
Ocular Complications in PHACE Syndrome: A True Association or a Coincidence?
Liat Samuelov, Michael Kinori, Anthony J Mancini, et al.
Fertility and Sterility
|
July 4, 2012
An embryo cleavage pattern based on the relative blastomere size as a function of cell number for predicting implantation outcome
Roee Sela, Liat Samuelov, Benny Almog, et al.
Experimental Dermatology
|
April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneity
Shahar Taiber, Liat Samuelov, Janan Mohamad, et al.
Experimental Dermatology
|
March 3, 2012
Calcitonin gene-related peptide (CGRP) may award relative protection from interferon-γ-induced collapse of human hair follicle immune privilege
Michael Kinori, Marta Bertolini, Wolfgang Funk, et al.
The British Journal of Dermatology
|
July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes
Janan Mohamad, Ofer Sarig, Paula Beattie, et al.
Page
of 7