Works matching AU Sprecher, E.

Results: 131

TCD evaluation before and after stenting in patients with severe primary carotid artery stenosis versus restenosis.

Published in:

2007

By:

Telman G;
Kouperberg E;
Sprecher E;
Gruberg L;
Beyar R;
Yarnitsky D;
Telman, Gregory;
Kouperberg, Efim;
Sprecher, Elliot;
Gruberg, Luis;
Beyar, Rafael;
Yarnitsky, David

Publication type:

journal article

Glutathione S-transferase T1-null seems to be associated with graft failure in hematopoietic SCT.

Published in:

Bone Marrow Transplantation, 2010, v. 45, n. 12, p. 1728, doi. 10.1038/bmt.2010.61

By:

Elhasid, R.;
Krivoy, N.;
Rowe, J. M.;
Sprecher, E.;
Efrati, E.

Publication type:

Article

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

Laryngeal mucous membrane pemphigoid serves as a prognostic factor for poor response to treatment with rituximab.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 5, p. 915, doi. 10.1111/ced.14662

By:

Baniel, A.;
Oestreicher‐Kedem, Y.;
Peled, A.;
Bar‐Ilan, E.;
Geller, S.;
Sprecher, E.;
Baum, S.

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

Bullous pemphigoid distributed above the injury level in a paraplegic patient.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 4, p. 531, doi. 10.1111/ced.14162

By:

Slutsky Bank, E.;
Baniel, A.;
Shehadeh, W.;
Gat, A.;
Matz, H.;
Ishii, N.;
Hashimoto, T.;
Sprecher, E.;
Zeeli, T.

Publication type:

Article

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.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 1, p. 41, doi. 10.1111/ced.14032

By:

Weinstein, A.;
Koren, A.;
Sprecher, E.;
Zur, E.;
Mehrabi, J. N.;
Artzi, O.

Publication type:

Article

Efficacy of a combination of diluted calcium hydroxylapatite‐based filler and an energy‐based device for the treatment of facial atrophic acne scars.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 5, p. e171, doi. 10.1111/ced.13952

By:

Koren, A.;
Isman, G.;
Cohen, S.;
Bar Ilan, E.;
Salameh, F.;
Sprecher, E.;
Artzi, O.

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

Grover disease and bullous pemphigoid: a clinicopathological study of six cases.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 5, p. 524, doi. 10.1111/ced.13789

By:

Ellenbogen, E.;
Geller, S.;
Azrielant, S.;
Zeeli, T.;
Goldberg, I.;
Schmidt, E.;
Zillikens, D.;
Mrowietz, U.;
Sherman, S.;
Mercer, S.;
Didkovsky, E.;
Hodak, E.;
Sprecher, E.

Publication type:

Article

Topical pimecrolimus for paediatric cutaneous mastocytosis.

Published in:

Clinical & Experimental Dermatology, 2018, v. 43, n. 5, p. 559, doi. 10.1111/ced.13391

By:

Mashiah, J.;
Harel, A.;
Bodemer, C.;
Hadj‐Rabia, S.;
Goldberg, I.;
Sprecher, E.;
Kutz, A.

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

Paraneoplastic pityriasis rubra pilaris: case report and literature review.

Published in:

Clinical & Experimental Dermatology, 2017, v. 42, n. 1, p. 54, doi. 10.1111/ced.13009

By:

Bar‐Ilan, E.;
Gat, A.;
Sprecher, E.;
Zeeli, T.

Publication type:

Article

A refractory, cutaneous, subepidermal bullous disease.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 5, p. 573, doi. 10.1111/ced.12823

By:

Geller, S.;
Gat, A.;
Zeeli, T.;
Schmidt, E.;
Ishii, N.;
Hashimoto, T.;
Zillikens, D.;
Sprecher, E.

Publication type:

Article

Isotretinoin treatment of autosomal recessive congenital ichthyosis complicated by coexisting dysferlinopathy.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 4, p. 390, doi. 10.1111/ced.12774

By:

Mashiah, J.;
Harel, A.;
Bitterman, O.;
Sagi, L.;
Gat, A.;
Fellig, Y.;
Ben‐Shachar, S.;
Sprecher, E.

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

Diffuse scalp alopecia in a middle-aged patient.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 8, p. 936, doi. 10.1111/ced.12091

By:

Samuelov, L.;
Arad, U.;
Gat, A.;
Pavlovsky, M.;
Sprecher, E.;
Matz, H.

Publication type:

Article

Reactive angioendotheliomatosis presenting as cellulitis.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 7, p. 748, doi. 10.1111/ced.12119

By:

Rozenblat, M.;
Pessach, Y.;
Gat, A.;
Bergman, R.;
Sprecher, E.;
Goldberg, I.

Publication type:

Article

Oesophageal involvement in bullous pemphigoid.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 3, p. 274, doi. 10.1111/j.1365-2230.2012.04408.x

By:

Maharshak, N.;
Sagi, M.;
Santos, E.;
Sprecher, E.;
Goldberg, I.

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

A 60-year-old woman with subcutaneous nodules on the thigh.

Published in:

Clinical & Experimental Dermatology, 2012, v. 37, n. 4, p. 448, doi. 10.1111/j.1365-2230.2011.04168.x

By:

Sagi, M.;
Marcus, B. S.;
Gat, A.;
Martinez de Morentin, H.;
Sprecher, E.;
Goldberg, I.

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

Chronic granulomatous disease of childhood: an unusual cause of recurrent uncommon infections in a 61-year-old man.

Published in:

Clinical & Experimental Dermatology, 2011, v. 36, n. 7, p. 759, doi. 10.1111/j.1365-2230.2011.04101.x

By:

Isman-Nelkenbaum, G.;
Wolach, B.;
Gavrieli, R.;
Roos, D.;
Sprecher, E.;
Bash, E.;
Gat, A.;
Sprecher, H.;
Ben-Ami, R.;
Zeeli, T.

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

A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.

Published in:

Clinical & Experimental Dermatology, 2011, v. 36, n. 2, p. 188, doi. 10.1111/j.1365-2230.2010.03944.x

By:

Nahum, S.;
Morice-Picard, F.;
Taieb, A.;
Sprecher, E.

Publication type:

Article

Novel mutations in DSG1 causing striate palmoplantar keratoderma.

Published in:

Clinical & Experimental Dermatology, 2009, v. 34, n. 2, p. 224, doi. 10.1111/j.1365-2230.2008.02733.x

By:

Hershkovitz, D.;
Lugassy, J.;
Indelman, M.;
Bergman, R.;
Sprecher, E.

Publication type:

Article

Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy.

Published in:

Clinical & Experimental Dermatology, 2007, v. 32, n. 2, p. 191, doi. 10.1111/j.1365-2230.2006.02335.x

By:

Indelman, M.;
Eason, J.;
Hummel, M.;
Loza, O.;
Suri, M.;
Leys, M. J.;
Bayne, M.;
Schwartz, F. L.;
Sprecher, E.

Publication type:

Article

Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.

Published in:

Clinical & Experimental Dermatology, 2005, v. 30, n. 1, p. 64, doi. 10.1111/j.1365-2230.2004.01661.x

By:

Tal, O.;
Bergman, R.;
Alcalay, J.;
Indelman, M.;
Sprecher, E.

Publication type:

Article

Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome.

Published in:

Clinical & Experimental Dermatology, 2004, v. 29, n. 5, p. 513, doi. 10.1111/j.1365-2230.2004.01589.x

By:

Sprecher, E.;
Tesfaye-Kedjela, A.;
Ratajczak, P.;
Bergman, R.;
Richard, G.

Publication type:

Article

Comparison of risk factors and work-up in young and middle-aged patients with TIA and ischaemic stroke.

Published in:

European Journal of Neurology, 2010, v. 17, n. 4, p. 567, doi. 10.1111/j.1468-1331.2009.02857.x

By:

Telman, G.;
Sprecher, E.;
Namestnikov, O.;
Kouperberg, E.

Publication type:

Article

Size of PFO and amount of microembolic signals in patients with ischaemic stroke or TIA.

Published in:

European Journal of Neurology, 2008, v. 15, n. 9, p. 969, doi. 10.1111/j.1468-1331.2008.02232.x

By:

Telman, G.;
Yalonetsky, S.;
Kouperberg, E.;
Sprecher, E.;
Lorber, A.;
Yarnitsky, D.

Publication type:

Article

Vesicular eruption located on sunburned areas in an 8-year-old girl.

Published in:

2009

By:

Zoller L;
Shavit I;
Sprecher E

Publication type:

Journal Article

Vesicular eruption located on sunburned areas in an 8-year-old girl (Case Presentation).

Published in:

Acta Paediatrica, 2009, v. 98, n. 11, p. 1706, doi. 10.1111/j.1651-2227.2009.01456.x

By:

Zoller, L.;
Shavit, I.;
Sprecher, E.

Publication type:

Article

Vesicular eruption located on sunburned areas in an 8-year-old girl (Discussion and Diagnosis).

Published in:

Acta Paediatrica, 2009, v. 98, n. 11, p. 1855, doi. 10.1111/j.1651-2227.2009.01457.x

By:

Zoller, L.;
Shavit, I.;
Sprecher, E.

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

Book Review: Lehrbuch der Pharmakognosie. Auf phytochemischer Grundlage (Textbook of pharmacognosy. On a phytochemical basis). By E. Steinegger and R. Hänsel.

Published in:

Angewandte Chemie International Edition, 1969, v. 8, n. 3, p. 223, doi. 10.1002/anie.196902234

By:

Sprecher, E.

Publication type:

Article

Nail dystrophy in focal acral hyperkeratosis: a distinctive feature?

Published in:

2008

By:

Khamaysi, Z.;
Bergman, R.;
Sprecher, E.

Publication type:

Letter

Familial palmoplantar keratoderma: not always hereditary.

Published in:

2007

By:

Khamaysi, Z.;
Indelman, M.;
Bergman, R.;
Sprecher, E.

Publication type:

Letter

Autonomic asymmetry in migraine: augmented parasympathetic activation in left unilateral migraineurs.

Published in:

2004

By:

Avnon Y;
Nitzan M;
Sprecher E;
Rogowski Z;
Yarnitsky D

Publication type:

Journal Article

Different patterns of parasympathetic activation in uni- and bilateral migraineurs.

Published in:

2003

By:

Avnon Y;
Nitzan M;
Sprecher E;
Rogowski Z;
Yarnitsky D

Publication type:

Journal Article

Different patterns of parasympathetic activation in uni- and bilateral migraineurs.

Published in:

Brain: A Journal of Neurology, 2003, v. 126, n. 7, p. 1660, doi. 10.1093/brain/awg158

By:

Y. Avnon;
M. Nitzan;
E. Sprecher;
Z. Rogowski;
D. Yarnitsky

Publication type:

Article