Works by Sarig, O.

Results: 39

Evidence for cutaneous dysbiosis in dystrophic epidermolysis bullosa.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 7, p. 1223, doi. 10.1111/ced.14592

By:

Bar, J.;
Sarig, O.;
Lotan‐Pompan, M.;
Dassa, B.;
Miodovnik, M.;
Weinberger, A.;
Sprecher, E.;
Segal, E.;
Samuelov, L.

Publication type:

Article

Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 5, p. 990, doi. 10.1111/ced.14575

By:

Vodo, D.;
Malchin, N.;
DeRowe, A.;
Sprecher, E.;
Sarig, O.

Publication type:

Article

Identification of clinically useful predictive genetic variants in pachyonychia congenita.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 5, p. 867, doi. 10.1111/ced.14569

By:

Samuelov, L.;
Sarig, O.;
Adir, N.;
Pavlovsky, M.;
Smith, F. J.;
Schwartz, J.;
Hansen, C. D.;
Sprecher, E.

Publication type:

Article

Molecular epidemiology of pachyonychia congenita in the Israeli population.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 4, p. 663, doi. 10.1111/ced.14509

By:

Pavlovsky, M.;
Peled, A.;
Samuelov, L.;
Malki, L.;
Malovitski, K.;
Assaf, S.;
Mohamad, J.;
Meijers, O.;
Eskin‐Schwartz, M.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 1, p. 103, doi. 10.1111/ced.14384

By:

Mohamad, J.;
Samuelov, L.;
Malki, L.;
Peled, A.;
Pavlovsky, M.;
Malovitski, K.;
Taiber, S.;
Adir, N.;
Rabinowitz, T.;
Shomron, N.;
Milner, J. D.;
Lestringant, G.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

PLACK syndrome shows remarkable phenotypic homogeneity.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 5, p. 580, doi. 10.1111/ced.13887

By:

Mohamad, J.;
Samuelov, L.;
Ben‐Amitai, D.;
Malchin, N.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location.

Published in:

Clinical & Experimental Dermatology, 2018, v. 43, n. 2, p. 187, doi. 10.1111/ced.13324

By:

Vodo, D.;
Sarig, O.;
Peled, A.;
Samuelov, L.;
Malchin, N.;
Grafi‐Cohen, M.;
Sprecher, E.

Publication type:

Article

A novel homozygous deletion in EXPH5 causes a skin fragility phenotype.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 8, p. 915, doi. 10.1111/ced.12908

By:

Malchin, N.;
Sarig, O.;
Grafi‐Cohen, M.;
Geller, S.;
Goldberg, I.;
Shani, A.;
Gat, A;
Sprecher, E.;
Mashiah, J.

Publication type:

Article

A case for diagnosis.

Published in:

Clinical & Experimental Dermatology, 2015, v. 40, n. 6, p. 697, doi. 10.1111/ced.12599

By:

Samuelov, L.;
Sarig, O.;
Goldsmith, T.;
Pavlovsky, M.;
Goldberg, I.;
Sagie, S.;
Selig, S.;
Sprecher, E.

Publication type:

Article

Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in the PSTPIP1 gene.

Published in:

Clinical & Experimental Dermatology, 2015, v. 40, n. 4, p. 367, doi. 10.1111/ced.12585

By:

Zeeli, T.;
Padalon‐Brauch, G.;
Ellenbogen, E.;
Gat, A.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome.

Published in:

Clinical & Experimental Dermatology, 2014, v. 39, n. 3, p. 361, doi. 10.1111/ced.12222

By:

Fuchs‐Telem, D.;
Nousbeck, J.;
Singer, A.;
McGrath, J. A.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family.

Published in:

Clinical & Experimental Dermatology, 2014, v. 39, n. 2, p. 182, doi. 10.1111/ced.12213

By:

Eytan, O.;
Sarig, O.;
Israeli, S.;
Mevorah, B.;
Basel‐Vanagaite, L.;
Sprecher, E.

Publication type:

Article

Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 8, p. 911, doi. 10.1111/ced.12148

By:

Israeli, S.;
Goldberg, I.;
Fuchs ‐ Telem, D.;
Bergman, R.;
Indelman, M.;
Bitterman ‐ Deutsch, O.;
Harel, A.;
Mashiach, Y.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 2, p. 189, doi. 10.1111/ced.12059

By:

Fuchs‐Telem, D.;
Padalon‐Brauch, G.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia.

Published in:

Clinical & Experimental Dermatology, 2012, v. 37, n. 2, p. 186, doi. 10.1111/j.1365-2230.2011.04135.x

By:

Pavlovsky, M.;
Fuchs-Telem, D.;
Nousbeck, J.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Beneficial effect of acitretin in Chanarin-Dorfman syndrome.

Published in:

Clinical & Experimental Dermatology, 2012, v. 37, n. 1, p. 31, doi. 10.1111/j.1365-2230.2011.04164.x

By:

Israeli, S.;
Pessach, Y.;
Sarig, O.;
Goldberg, I.;
Sprecher, E.

Publication type:

Article

Erythrokeratoderma variabilis caused by a recessive mutation in GJB3.

Published in:

Clinical & Experimental Dermatology, 2011, v. 36, n. 4, p. 406, doi. 10.1111/j.1365-2230.2010.03986.x

By:

Fuchs-Telem, D.;
Pessach, Y.;
Mevorah, B.;
Shirazi, I.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

APERIODICITY OF COCYCLES AND CONDITIONAL LOCAL LIMIT THEOREMS.

Published in:

Stochastics & Dynamics, 2004, v. 4, n. 1, p. 31, doi. 10.1142/S0219493704000936

By:

Aaronson, J.;
Denker, M.;
Sarig, O.;
Zweimüller, R.

Publication type:

Article

An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family.

Published in:

British Journal of Dermatology, 2011, v. 164, n. 6, p. 1390, doi. 10.1111/j.1365-2133.2011.10252.x

By:

Samuelov, L.;
Fuchs-Telem, D.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

CEDNIK syndrome results from loss-of-function mutations in SNAP29.

Published in:

British Journal of Dermatology, 2011, v. 164, n. 3, p. 610, doi. 10.1111/j.1365-2133.2010.10133.x

By:

Fuchs-Telem, D.;
Stewart, H.;
Rapaport, D.;
Nousbeck, J.;
Gat, A.;
Gini, M.;
Lugassy, Y.;
Emmert, S.;
Eckl, K.;
Hennies, H.C.;
Sarig, O.;
Goldsher, D.;
Meilik, B.;
Ishida-Yamamoto, A.;
Horowitz, M.;
Sprecher, E.

Publication type:

Article

The demand for stocks: an analysis of IPO auctions.

Published in:

Review of Financial Studies, 1999, v. 12, n. 2, doi. 10.1093/rfs/12.2.227

By:

Kandel, S;
Kandel, Shmuel;
Sarig, O;
Sarig, Oded;
Wohl, A;
Wohl, Avi

Publication type:

Article

Taxes and capital structure: evidence from firms' response to the Tax Reform Act of 1986.

Published in:

Review of Financial Studies, 1992, v. 5, n. 2, doi. 10.1093/rfs/5.2.331

By:

Givoly, D;
Givoly, Dan;
Hayn, C;
Hayn, Carla;
Ofer, AR;
Ofer, Aharon R.;
Sarig, O;
Sarig, Oded

Publication type:

Article

ST18 affects cell–cell adhesion in pemphigus vulgaris in a tumour necrosis factor‐α‐dependent fashion.

Published in:

British Journal of Dermatology, 2021, v. 184, n. 6, p. 1153, doi. 10.1111/bjd.19679

By:

Assaf, S.;
Malki, L.;
Mayer, T.;
Mohamad, J.;
Peled, A.;
Pavlovsky, M.;
Malovitski, K.;
Sarig, O.;
Vodo, D.;
Sprecher, E.

Publication type:

Article

Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome.

Published in:

British Journal of Dermatology, 2020, v. 183, n. 4, p. 756, doi. 10.1111/bjd.19123

By:

Ralser, D.J.;
Kumar, S.;
Borisov, O.;
Sarig, O.;
Richard, G.;
Wolf, S.;
Krawitz, P.M.;
Sprecher, E.;
Kreiß, M.;
Betz, R.C.

Publication type:

Article

Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.

Published in:

British Journal of Dermatology, 2020, v. 183, n. 1, p. 114, doi. 10.1111/bjd.18718

By:

Peled, A.;
Samuelov, L.;
Sarig, O.;
Bochner, R.;
Malki, L.;
Pavlovsky, M.;
Pichinuk, E.;
Weil, M.;
Sprecher, E.

Publication type:

Article

Treatment of epidermolysis bullosa pruriginosa‐associated pruritus with dupilumab.

Published in:

British Journal of Dermatology, 2020, v. 182, n. 6, p. 1495, doi. 10.1111/bjd.18855

By:

Shehadeh, W.;
Sarig, O.;
Bar, J.;
Sprecher, E.;
Samuelov, L.

Publication type:

Article

Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey–Hailey disease are allelic disorders.

Published in:

British Journal of Dermatology, 2018, v. 179, n. 4, p. 1001, doi. 10.1111/bjd.16915

By:

Malchin, N.;
Furman, M.;
Sarig, O.;
Vodo, D.;
Sprecher, E.

Publication type:

Article

Striate palmoplantar keratoderma resulting from a missense mutation in DSG1.

Published in:

2018

By:

Vodo, D.;
O'Toole, E. A.;
Malchin, N.;
Lahav, A.;
Adir, N.;
Sarig, O.;
Green, K. J.;
Smith, F. J. D.;
Sprecher, E.

Publication type:

Case Study

Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype.

Published in:

2018

By:

Vodo, D.;
Sarig, O.;
Jeddah, D.;
Malchin, N.;
Eskin‐Schwarz, M.;
Mohamad, J.;
Rabinowitz, T.;
Goldberg, I.;
Shomron, N.;
Khamaysi, Z.;
Bergman, R.;
Sprecher, E.

Publication type:

Letter to the Editor

Novel <italic>POFUT1</italic> 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.

Published in:

2018

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Hafner, A.;
Sprecher, E.

Publication type:

Letter to the Editor

由PSENEN始祖突变引起的结合了化脓性汗腺炎与道林‐德戈斯(Dowling–Degos)病的表现型

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. e177, doi. 10.1111/bjd.16303

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Malchin, N.;
Bochner, R.;
Mohamad, J.;
Gat, A.;
Peled, A.;
Hafner, A.;
Sprecher, E.

Publication type:

Article

A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. e160, doi. 10.1111/bjd.16285

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Malchin, N.;
Bochner, R.;
Mohamad, J.;
Gat, A.;
Peled, A.;
Hafner, A.;
Sprecher, E.

Publication type:

Article

A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. 502, doi. 10.1111/bjd.16000

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Malchin, N.;
Bochner, R.;
Mohamad, J.;
Gat, A.;
Peled, A.;
Hafner, A.;
Sprecher, E.

Publication type:

Article

Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.

Published in:

British Journal of Dermatology, 2016, v. 175, n. 1, p. 178, doi. 10.1111/bjd.14425

By:

Khamaysi, Z.;
Bochner, R.;
Indelman, M.;
Magal, L.;
Avitan ‐ Hersh, E.;
Sarig, O.;
Sprecher, E.;
Bergman, R.

Publication type:

Article

Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10.

Published in:

British Journal of Dermatology, 2015, v. 173, n. 1, p. 293, doi. 10.1111/bjd.13616

By:

Samuelov, L.;
Sarig, O.;
Gat, A.;
Halachmi, S.;
Shalev, S.;
Sprecher, E.

Publication type:

Article

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.

Published in:

British Journal of Dermatology, 2014, v. 171, n. 6, p. 1521, doi. 10.1111/bjd.13176

By:

Nousbeck, J.;
Sarig, O.;
Magal, L.;
Warshauer, E.;
Burger, B.;
Itin, P.;
Sprecher, E.

Publication type:

Article

Clinical response to ustekinumab in familial pityriasis rubra pilaris caused by a novel mutation in CARD14.

Published in:

British Journal of Dermatology, 2014, v. 171, n. 2, p. 420, doi. 10.1111/bjd.12952

By:

Eytan, O.;
Sarig, O.;
Sprecher, E.;
Steensel, M.A.M.

Publication type:

Article

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris.

Published in:

British Journal of Dermatology, 2014, v. 170, n. 5, p. 1196, doi. 10.1111/bjd.12799

By:

Eytan, O.;
Qiaoli, L.;
Nousbeck, J.;
Steensel, M.A.M.;
Burger, B.;
Hohl, D.;
Taïeb, A.;
Prey, S.;
Bachmann, D.;
Avitan‐Hersh, E.;
Jin Chung, H.;
Shemer, A.;
Trau, H.;
Bergman, R.;
Fuchs‐Telem, D.;
Warshauer, E.;
Israeli, S.;
Itin, P.H.;
Sarig, O.;
Uitto, J.

Publication type:

Article

Immune‐regulatory genes as possible modifiers of familial pityriasis rubra pilaris – lessons from a family with PRP and psoriasis.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2018, v. 32, n. 10, p. e389, doi. 10.1111/jdv.15029

By:

Spoerri, I.;
Burger, B.;
Itin, P.H.;
Herms, S.;
Heinimann, K.;
Eytan, O.;
Sarig, O.;
Sprecher, E.

Publication type:

Article