Eli Sprecher (E Sprecher)

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 28

Top Topics

Hidradenitis Suppurativa

Top Venues

The British journal of dermatology

Clinical and experimental dermatology

Experimental dermatology

Pediatric dermatology

This page only lists publications with an associated author ORCID identifier.

Publications

Shir Bergson, Daniel Daniely, David Bomze, Janan Mohamad, Kiril Malovitski, Odile Meijers, Valeria Briskin, Ofer Bihari, Natalia Malchin, Shirli Israeli, Jacob Mashiah, Tzipora Falik-Zaccai, Emily Avitan-Hersh, Marina Eskin-Schwartz, Stavit Allon-Shalev, Ofer Sarig, Eli Sprecher, Liat Samuelov
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa. Pediatric dermatology (2023)
Alon Peled, Ofer Sarig, Janan Mohamad, Marina Eskin-Schwartz, Dan Vodo, Ron Bochner, Natalia Malchin, Ofer Isakov, Noam Shomron, Gilad Fainberg, Marta Bertolini, Ralf Paus, Eli Sprecher
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4. American journal of medical genetics. Part A (2023)
Janan Mohamad, Ofer Sarig, Paula Beattie, Kiril Malovitski, Sari Assaf, Edel O'Toole, Janice Schwartz, Holly Evans, Liat Samuelov, Eli Sprecher
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes. The British journal of dermatology 187 (5) (2022)
Eli Sprecher
What do rare and common have in common? The British journal of dermatology 187 (3) (2022)
Janan Mohamad, Liat Samuelov, Sari Assaf, Liron Malki, Kiril Malovitski, Odile Meijers, Noam Adir, Ester Granot, Mali Barbi, Ofer Sarig, Eli Sprecher
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1. American journal of medical genetics. Part A 188 (10) (2022)
Kiril Malovitski, Odile Meijers, Eran Cohen-Barak, James Bergman, Noam Adir, Moshe Giladi, Stavit Shalev, Ofer Sarig, Janice Schwartz, Holly Evans, Eli Sprecher, Liat Samuelov
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy. The British journal of dermatology 187 (5) (2022)
Janan Mohamad, Liat Samuelov, Natalia Malchin, Tom Rabinowitz, Sari Assaf, Liron Malki, Kiril Malovitski, Shirli Israeli, Meital Grafi-Cohen, Ora Bitterman-Deutsch, Vered Molho-Pessach, Eran Cohen-Barak, Gideon Bach, Ben Zion Garty, Reuven Bergman, Avikam Harel, Arti Nanda, Giles G Lestringant, John A McGrath, Stavit Shalev, Noam Shomron, Jacob Mashiah, Marina Eskin-Schwartz, Eli Sprecher, Ofer Sarig
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population. Experimental dermatology 30 (9) (2021)
S Assaf, L Malki, T Mayer, J Mohamad, A Peled, M Pavlovsky, K Malovitski, Ofer Sarig, D Vodo, Eli Sprecher
ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashion. The British journal of dermatology 184 (6) (2021)
Dalit Ganani, Kiril Malovitski, Ofer Sarig, Andrea Gat, Eli Sprecher, Liat Samuelov
Epidermolysis bullosa simplex due to bi-allelic DST mutations: Case series and review of the literature. Pediatric dermatology 38 (2) (2021)
Liat Samuelov, Ron Bochner, Lee Magal, Kiril Malovitski, Nadav Sagiv, Janna Nousbeck, Aviad Keren, Dana Fuchs-Telem, Ofer Sarig, Amos Gilhar, Eli Sprecher
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis. Experimental dermatology (2021)
Janan Mohamad, Liat Samuelov, Sari Assaf, Dan Vodo, Ofer Sarig, Eli Sprecher
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2. Pediatric dermatology 38 (2) (2021)
J Mohamad, Liat Samuelov, L Malki, A Peled, M Pavlovsky, K Malovitski, S Taiber, N Adir, T Rabinowitz, N Shomron, J D Milner, G Lestringant, Ofer Sarig, Eli Sprecher
Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B. Clinical and experimental dermatology 46 (1) (2020)
Janan Mohamad, Arti Nanda, Mali Barbi, Alon Peled, Natalia Malchin, Kiril Malovitski, Rashida Pramanik, Daphna Weissglas-Volkov, Noam Shomron, John McGrath, Eli Sprecher, Ofer Sarig
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. Experimental dermatology 29 (8) (2020)
Pascal Joly, B Horvath, Α Patsatsi, Soner Uzun, R Bech, S Beissert, R Bergman, P Bernard, Luca Borradori, M Caproni, F Caux, G Cianchini, Maryam Danespazhooh, Dipankar De, Marian Dmochowski, Kossara Drenovska, J Ehrchen, Claudio Feliciani, Matthias Goebeler, R Groves, Claudia Günther, Silke C Hofmann, D Ioannides, C Kowalewski, Pardis-Sadat Tabatabaei-Panah, Y L Lim, B Marinovic, Angelo Valerio Marzano, Josè Manuel Mascarò, Daniel Mimouni, Dedee Frances Murrell, Carlo Pincelli, C P Squarcioni, M Sárdy, Jane F Setterfield, Eli Sprecher, Snejina Vassileva, K Wozniak, Savaş Yayli, G Zambruno, D Zillikens, M Hertl, Enno Schmidt
Updated S2K guidelines on the management of pemphigus vulgaris and foliaceus initiated by the european academy of dermatology and venereology (EADV). Journal of the European Academy of Dermatology and Venereology : JEADV 34 (9) (2020)
Liron Malki, Ofer Sarig, Nicole Cesarato, Janan Mohamad, Talia Canter, Sari Assaf, Mor Pavlovsky, Dan Vodo, Yossi Anis, Ofer Bihari, Kiril Malovitski, Andrea Gat, Holger Thiele, Bethany E Perez White, Liat Samuelov, Arti Nanda, Amy S Paller, Regina C Betz, Eli Sprecher
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Genetics in medicine : official journal of the American College of Medical Genetics 22 (7) (2020)
Shahar Taiber, Liat Samuelov, Janan Mohamad, Eran Cohen Barak, Ofer Sarig, Stavit Allon Shalev, Gilles Lestringant, Eli Sprecher
SAM syndrome is characterized by extensive phenotypic heterogeneity. Experimental dermatology 27 (7) (2019)
I Goldberg, Jacob Mashiah, A Kutz, A Derowe, E Warshauer, M E Schwartz, F Smith, Eli Sprecher, C D Hansen
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children. The British journal of dermatology 182 (3) (2019)
Amir Koren, G Isman, S Cohen, E Bar Ilan, F Salameh, Eli Sprecher, Ofir Artzi
Efficacy of a combination of diluted calcium hydroxylapatite-based filler and an energy-based device for the treatment of facial atrophic acne scars. Clinical and experimental dermatology 44 (5) (2019)
A Peled, Liat Samuelov, O Sarig, R Bochner, L Malki, M Pavlovsky, E Pichinuk, M Weil, Eli Sprecher
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. The British journal of dermatology 183 (1) (2019)
Amir Koren, Eli Sprecher, E Reider, Ofir Artzi
A treatment protocol for botulinum toxin injections in the treatment of pachyonychia congenita-associated keratoderma. The British journal of dermatology 182 (3) (2019)
J Mohamad, Liat Samuelov, D Ben-Amitai, N Malchin, O Sarig, Eli Sprecher
PLACK syndrome shows remarkable phenotypic homogeneity. Clinical and experimental dermatology 44 (5) (2019)
A Weinstein, A Koren, Eli Sprecher, E Zur, J N Mehrabi, Ofir Artzi
The combined effect of tranilast 8% liposomal gel on the final cosmesis of acne scarring in patients concomitantly treated by isotretinoin: prospective, double-blind, split-face study. Clinical and experimental dermatology 45 (1) (2019)
D Vodo, E A O'Toole, N Malchin, A Lahav, N Adir, O Sarig, K J Green, F J D Smith, Eli Sprecher
Striate palmoplantar keratoderma resulting from a missense mutation in DSG1. The British journal of dermatology 179 (3) (2018)
D Vodo, N Malchin, M Furman, O Sarig, Eli Sprecher
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disorders. The British journal of dermatology 179 (4) (2018)
M Pavlovsky, O Sarig, M Eskin-Schwartz, A Hafner, Eli Sprecher
Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors. The British journal of dermatology 178 (4) (2018)
D Vodo, O Sarig, D Jeddah, N Malchin, M Eskin-Schwarz, J Mohamad, T Rabinowitz, I Goldberg, N Shomron, Z Khamaysi, R Bergman, Eli Sprecher
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype. The British journal of dermatology 178 (6) (2018)
D Vodo, O Sarig, A Peled, Liat Samuelov, N Malchin, M Grafi-Cohen, Eli Sprecher
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location. Clinical and experimental dermatology 43 (2) (2017)
M Pavlovsky, O Sarig, M Eskin-Schwartz, N Malchin, R Bochner, J Mohamad, A Gat, A Peled, A Hafner, Eli Sprecher
A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN. The British journal of dermatology 178 (2) (2017)