Works matching AU Sprecher, Eli

Results: 172

Management of congenital ichthyoses: guidelines of care: Part two: 2024 update Free.

Published in:

British Journal of Dermatology, 2025, v. 193, n. 1, p. 28, doi. 10.1093/bjd/ljaf077

By:

Mazereeuw-Hautier, Juliette;
Paller, Amy S;
O'Toole, Edel;
Dreyfus, Isabelle;
Bodemer, Christine;
Akiyama, Masashi;
Diociaiuti, Andrea;
Hachem, Maya El;
Fischer, Judith;
Gonzalez-Sarmiento, Rogelio;
Gutiérrez-Cerrajero, Carlos;
Ott, Hagen;
Has, Cristina;
Jonca, Nathalie;
Tournier, Céline Granier;
Martinez, Ana;
Traupe, Heiko;
Salavastru, Carmen Maria;
Schmuth, Matthias;
Sprecher, Eli

Publication type:

Article

Management of congenital ichthyoses: guidelines of care: Part one: 2024 update Free.

Published in:

British Journal of Dermatology, 2025, v. 193, n. 1, p. 16, doi. 10.1093/bjd/ljaf076

By:

Mazereeuw-Hautier, Juliette;
Paller, Amy S;
Dreyfus, Isabelle;
Sprecher, Eli;
O'Toole, Edel;
Bodemer, Christine;
Akiyama, Masashi;
Diociaiuti, Andrea;
Hachem, Maya El;
Fischer, Judith;
Gonzalez-Sarmiento, Rogelio;
Gutiérrez-Cerrajero, Carlos;
Ott, Hagen;
Has, Cristina;
Jonca, Nathalie;
Tournier, Céline Granier;
Milesi, Sarah;
Texier, Hélène;
Martinez, Ana;
Traupe, Heiko

Publication type:

Article

Beyond Classification: A Unique Case of Self‐Resolving Cutaneous Mucinosis Associated With Streptococcal Infection in a Child.

Published in:

Pediatric Dermatology, 2025, v. 42, n. 3, p. 625, doi. 10.1111/pde.15856

By:

Safir, Ari;
Furman, Moran;
Gat, Andrea;
Zemser, Valentina;
Bergman, Reuven;
Sprecher, Eli;
Samuelov, Liat;
Friedel, Nadav

Publication type:

Article

Distribution of TPMT risk alleles for thioupurine toxicity in the Israeli population.

Published in:

European Journal of Clinical Pharmacology, 2009, v. 65, n. 3, p. 257, doi. 10.1007/s00228-008-0590-7

By:

Efrati, Edna;
Adler, Lior;
Krivoy, Norberto;
Sprecher, Eli

Publication type:

Article

Successful treatment of Schamberg’s disease with fractional non-ablative 1540 nm erbium:glass laser.

Published in:

Journal of Cosmetic & Laser Therapy, 2018, v. 20, n. 5, p. 265, doi. 10.1080/14764172.2017.1418513

By:

Hilerowicz, Yuval;
Sprecher, Eli;
Gat, Andrea;
Artzi, Ofir

Publication type:

Article

ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation.

Published in:

Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00770

By:

Radeva, Mariya Y.;
Walter, Elias;
Stach, Ramona Alexandra;
Yazdi, Amir S.;
Schlegel, Nicolas;
Sarig, Ofer;
Sprecher, Eli;
Waschke, Jens

Publication type:

Article

Tinea capitis outbreak among paediatric refugee population, an evolving healthcare challenge.

Published in:

Mycoses, 2016, v. 59, n. 9, p. 553, doi. 10.1111/myc.12501

By:

Mashiah, Jacob;
Kutz, Ana;
Ben Ami, Ronen;
Savion, Mihal;
Goldberg, Ilan;
Gan Or, Tamar;
Zidan, Omri;
Sprecher, Eli;
Harel, Avikam

Publication type:

Article

Anterior Scleritis Associated with Pemphigus Vulgaris.

Published in:

2019

By:

Zeeli, Tal;
Bar-Ilan, Efrat;
Sprecher, Eli;
Habot-Wilner, Zohar

Publication type:

Case Study

Superimposed type 2 segmental atopic dermatitis: case series and review of the literature.

Published in:

Clinical & Experimental Dermatology, 2022, v. 47, n. 9, p. 1703, doi. 10.1111/ced.15196

By:

Bar‐Ilan, Efrat;
Mashiah, Jacob;
Alkalay, Ronen;
Ingber, Arieh;
Zahavi, Keren Or;
Bar, Jonathan;
Zeeli, Tal;
Gat, Andrea;
Samuelov, Liat;
Sprecher, Eli;
Goldberg, Ilan

Publication type:

Article

A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome.

Published in:

Clinical & Experimental Dermatology, 2006, v. 31, n. 3, p. 435, doi. 10.1111/j.1365-2230.2006.02112.x

By:

Hershkovitz, T.;
Hassoun, G.;
Indelman, M.;
Shlush, L. I.;
Bergman, R.;
Pollack, S.;
Sprecher, Eli

Publication type:

Article

Diffuse Facial Hyperpigmentation as a Presenting Sign of Lupus Erythematosus: Three Cases and Review of the Literature.

Published in:

Case Reports in Dermatology, 2021, v. 13, n. 2, p. 263, doi. 10.1159/000515732

By:

Azrielant, Shir;
Ellenbogen, Eran;
Peled, Alon;
Zemser-Werner, Valentina;
Samuelov, Liat;
Sprecher, Eli;
Pavlovsky, Mor

Publication type:

Article

Human telomerase RNA component expression in Spitz nevi, common melanocytic nevi, and malignant melanomas.

Published in:

Journal of Cutaneous Pathology, 2002, v. 29, n. 6, p. 341, doi. 10.1034/j.1600-0560.2002.290603.x

By:

Guttman-Yassky, Emma;
Bergman, Reuven;
Manov, Lena;
Sprecher, Eli;
Shaefer, Yan;
Kerner, Hedviga

Publication type:

Article

Apoptosis, Fas and Fas-ligand expression in melanocytic tumors.

Published in:

Journal of Cutaneous Pathology, 1999, v. 26, n. 2, p. 72, doi. 10.1111/j.1600-0560.1999.tb01805.x

By:

Sprecher, Eli;
Bergman, Reuven;
Meilick, Ahuvah;
Kerner, Hedviga;
Manov, Lena;
Reiter, Irena;
Shafer, Yan;
Maor, Gilah;
Friedman-Birnbaum, Rachel

Publication type:

Article

Disentangling the roots of inherited hair disorders.

Published in:

Nature Genetics, 2008, v. 40, n. 3, p. 265, doi. 10.1038/ng0308-265

By:

Sprecher, Eli

Publication type:

Article

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

Published in:

Nature Genetics, 2004, v. 36, n. 6, p. 579, doi. 10.1038/ng1358

By:

Topaz, Orit;
Shurman, Daniel L.;
Bergman, Reuven;
Indelman, Margarita;
Ratajczak, Paulina;
Mizrachi, Mordechai;
Khamaysi, Ziad;
Behar, Doron;
Petronius, Dan;
Friedman, Vered;
Zelikovic, Israel;
Raimer, Sharon;
Metzker, Arieh;
Richard, Gabriele;
Sprecher, Eli

Publication type:

Article

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.

Published in:

Nature Genetics, 2001, v. 29, n. 2, p. 134, doi. 10.1038/ng716

By:

Sprecher, Eli;
Bergman, Reuven;
Richard, Gabriele;
Lurie, Raziel;
Shalev, Stavit;
Petronius, Dan;
Shalata, Adel;
Anbinder, Yefim;
Leibu, Rina;
Perlman, Ido;
Cohen, Nadine;
Szargel, Raymonde

Publication type:

Article

Concomitant Occurrence of Pyoderma Gangrenosum and Erythema Nodosum in Inflammatory Bowel Disease.

Published in:

Israel Medical Association Journal, 2014, v. 16, n. 3, p. 168

By:

Goldberg, Ilan;
Finkel, Oksana;
Gat, Andrea;
Sprecher, Eli;
de Morentin, Helena Martinez

Publication type:

Article

A systematic review of US state environmental legislation and regulation with regards to the prevention of neurodevelopmental disabilities and asthma.

Published in:

2009

By:

Zajac L;
Sprecher E;
Landrigan PJ;
Trasande L;
Zajac, Lauren;
Sprecher, Eli;
Landrigan, Philip J;
Trasande, Leonardo

Publication type:

journal article

A systematic review of US state environmental legislation and regulation with regards to the prevention of neurodevelopmental disabilities and asthma.

Published in:

Environmental Health: A Global Access Science Source, 2009, v. 8, p. 1, doi. 10.1186/1476-069X-8-9

By:

Zajc, Lauren;
Sprecher, Eli;
Landrigan, Philip J.;
Trasande, Leonardo

Publication type:

Article

SNG100, a novel topical treatment for moderate atopic dermatitis, in patients aged 6 years or older: A randomised, double‐blind, active‐controlled trial.

Published in:

Skin Health & Disease, 2023, v. 3, n. 6, p. 1, doi. 10.1002/ski2.293

By:

Samuelov, Liat;
Shemer, Avner;
Greenberger, Shoshana;
Ziv, Inbal;
Friedman, Doron;
Yacoby‐Zeevi, Oron;
Dodiuk‐Gad, Roni;
Ramot, Yuval;
Murad, Sari;
Sprecher, Eli

Publication type:

Article

Short-Term Safety of Booster Immunization With BNT162b2 mRNA COVID-19 Vaccine in Healthcare Workers.

Published in:

Open Forum Infectious Diseases, 2022, v. 9, n. 3, p. 1, doi. 10.1093/ofid/ofab656

By:

Paran, Yael;
Saiag, Esther;
Spitzer, Avishay;
Angel, Yoel;
Yakubovsky, Michal;
Padova, Hagit;
Ben-Ami, Ronen;
Goldinger, Ilana;
Gamzu, Ronni;
Sprecher, Eli;
Zeltser, David;
Henig, Oryan

Publication type:

Article

Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis.

Published in:

Experimental Dermatology, 2022, v. 31, n. 4, p. 567, doi. 10.1111/exd.14502

By:

Samuelov, Liat;
Bochner, Ron;
Magal, Lee;
Malovitski, Kiril;
Sagiv, Nadav;
Nousbeck, Janna;
Keren, Aviad;
Fuchs‐Telem, Dana;
Sarig, Ofer;
Gilhar, Amos;
Sprecher, Eli

Publication type:

Article

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.

Published in:

Experimental Dermatology, 2020, v. 29, n. 8, p. 742, doi. 10.1111/exd.14140

By:

Mohamad, Janan;
Nanda, Arti;
Pavlovsky, Mor;
Peled, Alon;
Malchin, Natalia;
Malovitski, Kiril;
Pramanik, Rashida;
Weissglas‐Volkov, Daphna;
Shomron, Noam;
McGrath, John;
Sprecher, Eli;
Sarig, Ofer

Publication type:

Article

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Published in:

Experimental Dermatology, 2018, v. 27, n. 7, p. 787, doi. 10.1111/exd.13551

By:

Taiber, Shahar;
Samuelov, Liat;
Mohamad, Janan;
Barak, Eran Cohen;
Sarig, Ofer;
Shalev, Stavit Allon;
Lestringant, Gilles;
Sprecher, Eli

Publication type:

Article

A distinct cutaneous microbiota profile in autoimmune bullous disease patients.

Published in:

Experimental Dermatology, 2017, v. 26, n. 12, p. 1221, doi. 10.1111/exd.13357

By:

Miodovnik, Mor;
Künstner, Axel;
Langan, Ewan A.;
Zillikens, Detlef;
Gläser, Regine;
Sprecher, Eli;
Baines, John F.;
Schmidt, Enno;
Ibrahim, Saleh M.

Publication type:

Article

Monopathogenic vs multipathogenic explanations of pemphigus pathophysiology.

Published in:

Experimental Dermatology, 2016, v. 25, n. 11, p. 839, doi. 10.1111/exd.13106

By:

Ahmed, A. Razzaque;
Carrozzo, Marco;
Caux, Frédéric;
Cirillo, Nicola;
Dmochowski, Marian;
Alonso, Agustín España;
Gniadecki, Robert;
Hertl, Michael;
López‐Zabalza, Maria J.;
Lotti, Roberta;
Pincelli, Carlo;
Pittelkow, Mark;
Schmidt, Enno;
Sinha, Animesh A.;
Sprecher, Eli;
Grando, Sergei A.

Publication type:

Article

Non-keratinocyte SNAP29 influences epidermal differentiation and hair follicle formation in mice.

Published in:

Experimental Dermatology, 2016, v. 25, n. 8, p. 647, doi. 10.1111/exd.13050

By:

Schiller, Stina A.;
Seebode, Christina;
Wieser, Georg L.;
Goebbels, Sandra;
Ruhwedel, Torben;
Horowitz, Mia;
Rapaport, Debora;
Sarig, Ofer;
Sprecher, Eli;
Emmert, Steffen

Publication type:

Article

Autosomal-dominant cutis laxa resulting from an intronic mutation in ELN.

Published in:

2015

By:

Vodo, Dan;
Sarig, Ofer;
Peled, Alon;
Frydman, Moshe;
Greenberger, Shoshi;
Sprecher, Eli

Publication type:

Case Study

Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09951-x

By:

Assaf, Sari;
Vodo, Dan;
Malovitski, Kiril;
Mohamad, Janan;
Bergson, Shir;
Feller, Yarden;
Malki, Liron;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article

Role of Patch Testing in Chronic Spontaneous Urticaria.

Published in:

Journal of Asthma & Allergy, 2021, v. 14, p. 1075, doi. 10.2147/JAA.S325657

By:

Bar, Jonathan;
Godlewicz, Sari;
Ingber, Arieh;
Sprecher, Eli;
Slodownik, Dan

Publication type:

Article

Loss of SNAP29 Impairs Endocytic Recycling and Cell Motility.

Published in:

PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009759

By:

Rapaport, Debora;
Lugassy, Yevgenia;
Sprecher, Eli;
Horowitz, Mia

Publication type:

Article

Improving Hospital Outpatient Clinics Appointment Schedules by Prediction Models.

Published in:

Journal of Medical Systems, 2023, v. 47, n. 1, p. 1, doi. 10.1007/s10916-022-01902-3

By:

Babayoff, Orel;
Shehory, Onn;
Geller, Shamir;
Shitrit-Niselbaum, Chen;
Weiss-Meilik, Ahuva;
Sprecher, Eli

Publication type:

Article

Cyclosporine treatment of psoriatic erythroderma complicated by bacterial sepsis.

Published in:

1999

By:

Sprecher, Eli;
Bergman, Reuven;
Friedman-Birn- Baum, Rachel

Publication type:

Letter

Influence of glutathione S-transferase A1, P1, M1, T1 polymorphisms on oral busulfan pharmacokinetics in children with congenital hemoglobinopathies undergoing hematopoietic stem cell transplantation.

Published in:

Pediatric Blood & Cancer, 2010, v. 55, n. 6, p. 1172, doi. 10.1002/pbc.22739

By:

Elhasid, Ronit;
Krivoy, Norberto;
Rowe, Jacob M.;
Sprecher, Eli;
Adler, Lior;
Elkin, Hela;
Efrati, Edna

Publication type:

Article

Transient Pruritic Erythema as a Forme Fruste of Solar Urticaria.

Published in:

Israel Medical Association Journal, 2020, v. 22, n. 4, p. 227

By:

Azrielant, Shir;
Khanimov, Israel;
Sprecher, Eli;
Ellenbogen, Eran

Publication type:

Article

Comparative Study of Frozen and Paraffin-Embedded Sections: Evaluation of Inflammatory Dermatoses.

Published in:

Israel Medical Association Journal, 2019, v. 21, n. 2, p. 82

By:

Ellenbogen, Eran;
Epshteyn, Shmuel;
Azrielant, Shir;
Pavlovski, Mor;
Gat, Andrea;
Sprecher, Eli;
Goldberg, Ilan

Publication type:

Article

Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndrome.

Published in:

Acta Orthopaedica, 2009, v. 80, n. 1, p. 131, doi. 10.1080/17453670902807482

By:

Gok, Faysal;
Chefetz, Ilana;
Indelman, Margarita;
Kocaoglu, Murat;
Sprecher, Eli

Publication type:

Article

Glutathione S‐transferase polymorphisms in patients with photosensitive and non‐photosensitive drug eruptions.

Published in:

Photodermatology, Photoimmunology & Photomedicine, 2019, v. 35, n. 4, p. 214, doi. 10.1111/phpp.12454

By:

Ben Ami, Tal;
Sarig, Ofer;
Sprecher, Eli;
Goldberg, Ilan

Publication type:

Article

Somatic Mosaicism for a 'Lethal' GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement.

Published in:

Pediatric Dermatology, 2016, v. 33, n. 3, p. 322, doi. 10.1111/pde.12848

By:

Eskin‐Schwartz, Marina;
Metzger, Yoav;
Peled, Alon;
Weissglas‐Volkov, Daphna;
Malchin, Natalia;
Gat, Andrea;
Vodo, Dan;
Mevorah, Baruch;
Shomron, Noam;
Sprecher, Eli;
Sarig, Ofer

Publication type:

Article

Childhood Pemphigus Foliaceus with Exclusive Immunoglobulin G Autoantibodies to Desmocollins.

Published in:

Pediatric Dermatology, 2016, v. 33, n. 1, p. e10, doi. 10.1111/pde.12729

By:

Geller, Shamir;
Gat, Andrea;
Harel, Avikam;
Mashiah, Jacob;
Zeeli, Tal;
Eming, Rüdiger;
Ishii, Norito;
Hertl, Michael;
Hashimoto, Takashi;
Sprecher, Eli

Publication type:

Article

New Syndrome of Congenital Circumferential Skin Folds Associated with Multiple Congenital Anomalies.

Published in:

Pediatric Dermatology, 2012, v. 29, n. 1, p. 89, doi. 10.1111/j.1525-1470.2011.01403.x

By:

Basel-Vanagaite, Lina;
Sprecher, Eli;
Gat, Andrea;
Merlob, Paul;
Albin-Kaplanski, Adi;
Konen, Osnat;
Solomon, Benjamin D.;
Muenke, Maximilian;
Grzeschik, Karl-H.;
Sirota, Lea

Publication type:

Article

ADULT Syndrome Caused by a Mutation Previously Associated with EEC Syndrome.

Published in:

Pediatric Dermatology, 2010, v. 27, n. 6, p. 643, doi. 10.1111/j.1525-1470.2010.01131.x

By:

Avitan-Hersh, Emily;
Indelman, Margarita;
Bergman, Reuven;
Sprecher, Eli

Publication type:

Article

Bazex–Dupre–Christol Syndrome.

Published in:

Pediatric Dermatology, 2006, v. 23, n. 3, p. 286, doi. 10.1111/j.1525-1470.2006.00237.x

By:

Torrelo, Antonio;
Sprecher, Eli;
Mediero, Imelda G.;
Bergman, Reuven;
Zambrano, Antonio

Publication type:

Article

Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindred.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 5, p. 487, doi. 10.1007/s10038-006-0377-6

By:

Specktor, Polina;
Cooper, John;
Indelman, Margarita;
Sprecher, Eli

Publication type:

Article

T-Cell Monoclonality in the Blood and the Skin Correlates With Poor Response to Treatment in Mycosis Fungoides.

Published in:

2023

By:

Geller, Shamir;
Tel-Dan, Shira F.;
Solar, Irit;
Sprecher, Eli;
Goldberg, Ilan

Publication type:

journal article

Primary Cutaneous B-Cell Lymphomas in Children and Adolescents: A SEER Population-Based Study.

Published in:

Clinical Lymphoma, Myeloma & Leukemia, 2021, v. 21, n. 12, p. e1000, doi. 10.1016/j.clml.2021.07.021

By:

Bomze, David;
Sprecher, Eli;
Goldberg, Ilan;
Samuelov, Liat;
Geller, Shamir

Publication type:

Article

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 12, p. 2806, doi. 10.1002/ajmg.a.63408

By:

Peled, Alon;
Sarig, Ofer;
Mohamad, Janan;
Eskin‐Schwartz, Marina;
Vodo, Dan;
Bochner, Ron;
Malchin, Natalya;
Isakov, Ofer;
Shomron, Noam;
Fainberg, Gilad;
Bertolini, Marta;
Paus, Ralf;
Sprecher, Eli

Publication type:

Article

Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2879, doi. 10.1002/ajmg.a.62924

By:

Mohamad, Janan;
Samuelov, Liat;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Meijers, Odile;
Adir, Noam;
Granot, Ester;
Pavlovsky, Mor;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh-Like Syndrome) caused by novel mutations in SERAC1.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 9, p. 2204, doi. 10.1002/ajmg.a.36059

By:

Sarig, Ofer;
Goldsher, Dorit;
Nousbeck, Janna;
Fuchs ‐ Telem, Dana;
CohEN ‐ KatsENelson, KsENya;
Iancu, Theodore C.;
Manov, IrENa;
Saada, Ann;
Sprecher, Eli;
Mandel, Hanna

Publication type:

Article

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

Published in:

PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006008

By:

Vodo, Dan;
Sarig, Ofer;
Geller, Shamir;
Ben-Asher, Edna;
Olender, Tsviya;
Bochner, Ron;
Goldberg, Ilan;
Nosgorodsky, Judith;
Alkelai, Anna;
Tatarskyy, Pavel;
Peled, Alon;
Baum, Sharon;
Barzilai, Aviv;
Ibrahim, Saleh M.;
Zillikens, Detlef;
Lancet, Doron;
Sprecher, Eli

Publication type:

Article