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Eran Cohen‐Barak

emek medical center

16H指数
60论文数
795被引数
收录论文 35
发表时间
Giant angiokeratoma circumscriptum naeviforme巨大环状血管角皮瘤痣样型
err2026-08-12
err0
PREAI
errAdam Aizek Grempel; Wael Zaina; Tomer Cohen; Michael Ziv; Eran Cohen-Barak
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CARMIL2 deficiency disrupts activation-induced metabolic reprogramming in T cells, and is partially rescued by glutamine supplementationCARMIL2缺陷会破坏T细胞中激活诱导的代谢重编程,并且可通过谷氨酰胺补充部分挽救。
err2025-07-28
err0
errOAAI
errMona Kabha; Maya Liaks-Bohnick; Fadia Zagairy; Orna Atar; Mira Hamed; Michael Ziv; Nada Danial-Farran; Morad Khayat; Orly Ishach; Yael Dinur-Schejter; Vered Molho-Pessach; Ido Somekh; Shirly Frizinsky; Efrat Bar-Ilan; Shoshana Greenberger; NaserEddin Adeeb; Raz Somech; Polina Stepansky; Noga Ron-Harel; Eran Cohen-Barak
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Real-world efficacy and safety of dupilumab for paediatric atopic dermatitis: a multicentre retrospective study
err2024-11-14
err0
PREAI
errPirov, Eitan; Molho-Pessach, Vered; Cohen-Barak, Eran; Levitt, Jen A. Barak; Barzilai, Aviv; Bar, Jonathan; Renert-Yuval, Yael; Bar-Ilan, Efrat; Friedland, Rivka; Greenberger, Shoshana
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Diagnosis, treatment, and long-term outcomes of pediatric pemphigus: a retrospective study at tertiary medical centers
err2024-05-31
err0
errOAAI
errRenert-Yuval, Yael; Baum, Sharon; Greenberger, Shoshana; Cohen-Barak, Eran; Oren-Shabtai, Meital; Ben-Amitai, Dan; Friedland, Rivka
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Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene
err2024-05-01
err1
PREAI
errAtzmony, Lihi; Zagairy, Fadia; Mawassi, Banan; Shehade, Majd; Tatour, Yasmin; Danial-Farran, Nada; Khayat, Morad; Warrour, Nassim; Dodiuk-Gad, Roni; Cohen-Barak, Eran
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Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality
err2024-02-28
err1
errOAAI
errAbu Hanna, Firas; Zehavi, Yoav; Cohen-Barak, Eran; Khayat, Morad; Warwar, Nasim; Shreter, Roni; Rodenburg, Richard J.; Spiegel, Ronen
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Treatment with Methotrexate in Infants and Toddlers with Atopic Dermatitis: A Retrospective Multi-Center Study
err2023-08-20
err2
errOAAI
errLevitt, Jen A. Barak; Alemi, Sima; Ollech, Ayelet; Reiss-Huss, Shiran; Sah, Mohammad; Renert-Yuval, Yael; Friedland, Rivka; Greenberger, Shoshana; Barak, Eran Cohen
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Epidermal stratification requires retromer-mediated desmoglein-1 recycling
err2022-12-01
err10
errOAAI
errHegazy, Marihan; Koetsier, Jennifer L.; Huffine, Amber L.; Broussard, Joshua A.; Godsel, Brendan M.; Cohen-Barak, Eran; Sprecher, Eli; Wolfgeher, Donald J.; Kron, Stephen J.; Godsel, Lisa M.; Green, Kathleen J.
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Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy
err2022-11-01
err2
PREAI
errMalovitski, Kiril; Meijers, Odile; Cohen-Barak, Eran; Bergman, James; Adir, Noam; Giladi, Moshe; Shalev, Stavit; Sarig, Ofer; Schwartz, Janice; Evans, Holly; Sprecher, Eli; Samuelov, Liat
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Potential di-genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex
err2022-08-23
err2
PREAI
errKoren, Tamar; Zagairy, Fadia; Tatour, Yasmin; Belhanes-Peled, Hila; Khayat, Morad; Krausz, Judit; Danial-Farran, Nada; Ziv, Michael; Cohen-Barak, Eran
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A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia
err2022-06-16
err3
PREAI
errCohen-Barak, Eran; Danial-Farran, Nada; Chervinsky, Elana; Alimi-Kasem, Ola; Zagairy, Fadia; Livneh, Ido; Mawassi, Bannan; Hreish, Maysa; Khayat, Morad; Lossos, Alexander; Meiner, Vardiella; Ehilevitch, Nina; Weiss, Karin; Shalev, Stavit
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Translational implications of Th17-skewed inflammation due to genetic deficiency of a cadherin stress sensor
err2022-02-01
err29
errOAAI
errGodsel, Lisa M.; Roth-Carter, Quinn R.; Koetsier, Jennifer L.; Tsoi, Lam C.; Huffine, Amber L.; Broussard, Joshua A.; Fitz, Gillian N.; Lloyd, Sarah M.; Kweon, Junghun; Burks, Hope E.; Hegazy, Marihan; Amagai, Saki; Harms, Paul W.; Xing, Xianying; Kirma, Joseph; Johnson, Jodi L.; Urciuoli, Gloria; Doglio, Lynn T.; Swindell, William R.; Awatramani, Rajeshwar; Sprecher, Eli; Bao, Xiaomin; Cohen-Barak, Eran; Missero, Caterina; Gudjonsson, Johann E.; Green, Kathleen J.
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Concomitant variants in NF1, LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitorNF1,LZTR1和pnaz基因的伴随变异可能有助于丛状神经纤维瘤的侵袭性,并需要用MEK抑制剂治疗
err2021-12-20
err3
PREAI
errCohen-Barak, Eran; Toledano-Alhadef, Hagit; Danial-Farran, Nada; Livneh, Ido; Mwassi, Banan; Hriesh, Maysa; Zagairy, Fadia; Gafni-Amsalem, Chen; Bashir, Husam; Khayat, Morad; Warrour, Nassim; Sher, Osnat; Marom, Daphna; Postovsky, Sergey; Dujovny, Tal; Ziv, Michael; Shalev, Stavit A.
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Acral peeling in Nagashima type palmo-plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion
err2021-08-17
err8
errOAAI
errCohen-Barak, Eran; Azzam, Wassim; Koetsier, Jennifer L.; Danial-Farran, Nada; Barcan, Moran; Hriesh, Maysa; Khayat, Morad; Edison, Natalia; Krausz, Judith; Gafni-Amsalem, Chen; Kubo, Akiharu; Godsel, Lisa M.; Ziv, Michael; Allon-Shalev, Stavit
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Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population
err2021-04-15
err17
PREAI
errMohamad, Janan; Samuelov, Liat; Malchin, Natalia; Rabinowitz, Tom; Assaf, Sari; Malki, Liron; Malovitski, Kiril; Israeli, Shirli; Grafi-Cohen, Meital; Bitterman-Deutsch, Ora; Molho-Pessach, Vered; Cohen-Barak, Eran; Bach, Gideon; Garty, Ben Zion; Bergman, Reuven; Harel, Avikam; Nanda, Arti; Lestringant, Giles G.; McGrath, John; Shalev, Stavit; Shomron, Noam; Mashiah, Jacob; Eskin-Schwartz, Marina; Sprecher, Eli; Sarig, Ofer
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An Update on the Cutaneous Manifestations of Darier Disease
err2021-03-09
err8
PREAI
errYeshurun, Algit; Ziv, Michael; Cohen-Barak, Eran; Vered, Shiraz; Rozenman, Dganit; Sah, Muhammad; Khayat, Morad; Polyakov, Olga; Amichai, Boaz; Zlotogorski, Abraham; Shalev, Stavit; Dodiuk-Gad, Roni P.
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Homozygote loss-of-function variants in the humanCOCHgene underlie hearing loss
err2020-09-16
err9
errOAAI
errDanial-Farran, Nada; Chervinsky, Elena; Nadar-Ponniah, Prathamesh T.; Cohen Barak, Eran; Taiber, Shahar; Khayat, Morad; Avraham, Karen B.; Shalev, Stavit A.
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The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome
err2020-03-01
err19
errOAAI
errCohen-Barak, Eran; Godsel, Lisa M.; Koetsier, Jennifer L.; Hegazy, Marihan; Kushnir-Grinbaum, Daniella; Hammad, Helwe; Danial-Farran, Nada; Harmon, Robert; Khayat, Morad; Bochner, Ron; Peled, Alon; Rozenblat, Mati; Krausz, Judit; Sarig, Ofer; Johnson, Jodi L.; Ziv, Michael; Shalev, Stavit A.; Sprecher, Eli; Green, Kathleen J.
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