Guideline-discordant care among females undergoing groin hernia repair: the importance of sex as a biologic variable
Ehlers, A. P., Thumma, J. R., Howard, R., Davidson, G. H., Waljee, J. F., Dimick, J. B., Telem, D. A.
Published in Hernia : the journal of hernias and abdominal wall surgery (01.06.2022)
Published in Hernia : the journal of hernias and abdominal wall surgery (01.06.2022)
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Journal Article
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
Saada, A, Shaag, A, Arnon, S, Dolfin, T, Miller, C, Fuchs-Telem, D, Lombes, A, Elpeleg, O
Published in Journal of medical genetics (01.12.2007)
Published in Journal of medical genetics (01.12.2007)
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Journal Article
Leaning in and moving forward: a call to action and review of diversity initiatives in SAGES
Qureshi, A. P., Johnson, S. M., Sylla, P., Pryor, A. D., Telem, D., Jones, D. B., Bingener-Casey, J., Feldman, L. S., Mellinger, J.
Published in Surgical endoscopy (01.08.2024)
Published in Surgical endoscopy (01.08.2024)
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Journal Article
CEDNIK syndrome results from loss-of-function mutations in SNAP29
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.
Published in British journal of dermatology (1951) (01.03.2011)
Published in British journal of dermatology (1951) (01.03.2011)
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Journal Article
Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population
Israeli, S., Goldberg, I., Fuchs-Telem, D., Bergman, R., Indelman, M., Bitterman-Deutsch, O., Harel, A., Mashiach, Y., Sarig, O., Sprecher, E.
Published in Clinical and experimental dermatology (01.12.2013)
Published in Clinical and experimental dermatology (01.12.2013)
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Journal Article
An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family
Samuelov, L., Fuchs-Telem, D., Sarig, O., Sprecher, E.
Published in British journal of dermatology (1951) (01.06.2011)
Published in British journal of dermatology (1951) (01.06.2011)
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Journal Article
Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris
Eytan, O., Qiaoli, L., Nousbeck, J., van 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., Sprecher, E.
Published in British journal of dermatology (1951) (01.05.2014)
Published in British journal of dermatology (1951) (01.05.2014)
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Journal Article
Human placental-derived adherent stromal cells co-induced with TNF-α and IFN-γ inhibit triple-negative breast cancer in nude mouse xenograft models
Allen, H, Shraga-Heled, N, Blumenfeld, M, Dego-Ashto, T, Fuchs-Telem, D, Gilert, A, Aberman, Z, Ofir, R
Published in Cytotherapy (Oxford, England) (01.05.2018)
Published in Cytotherapy (Oxford, England) (01.05.2018)
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Journal Article
Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9
Fuchs-Telem, D., Padalon-Brauch, G., Sarig, O., Sprecher, E.
Published in Clinical and experimental dermatology (01.03.2013)
Published in Clinical and experimental dermatology (01.03.2013)
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Journal Article
Erythrokeratoderma variabilis caused by a recessive mutation in GJB3
Fuchs-Telem, D., Pessach, Y., Mevorah, B., Shirazi, I., Sarig, O., Sprecher, E.
Published in Clinical and experimental dermatology (01.06.2011)
Published in Clinical and experimental dermatology (01.06.2011)
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Journal Article
67 - Human placental-derived adherent stromal cells co-induced with TNF-α and IFN-γ inhibit triple-negative breast cancer in nude mouse xenograft models
Allen, H., Shraga-Heled, N., Blumenfeld, M., Dego-Ashto, T., Fuchs-Telem, D., Gilert, A., Aberman, Z., Ofir, R.
Published in Cytotherapy (Oxford, England) (01.05.2018)
Published in Cytotherapy (Oxford, England) (01.05.2018)
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Journal 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 S epsilon RAC1
Sarig, O, Goldsher, D, Nousbeck, J, Fuchs-Telem, D, Cohen-Katsenelson, K, Iancu, T C, Manov, I, Saada, A, Sprecher, E, Mandel, H
Published in American journal of medical genetics. Part A (01.09.2013)
Published in American journal of medical genetics. Part A (01.09.2013)
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Journal Article
RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome
Basel-Vanagaite, Lina, Sarig, Ofer, Hershkovitz, Dov, Fuchs-Telem, Dana, Rapaport, Debora, Gat, Andrea, Isman, Gila, Shirazi, Idit, Shohat, Mordechai, Enk, Claes D., Birk, Efrat, Kohlhase, Jürgen, Matysiak-Scholze, Uta, Maya, Idit, Knopf, Carlos, Peffekoven, Anette, Hennies, Hans-Christian, Bergman, Reuven, Horowitz, Mia, Ishida-Yamamoto, Akemi, Sprecher, Eli
Published in American journal of human genetics (14.08.2009)
Published in American journal of human genetics (14.08.2009)
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Journal Article
Minimally invasive surgery for splenic malignancies
Telem, D, Chin, E H, Colon, M, Nguyen, S Q, Weber, K, Divino, C M
Published in Minerva chirurgica (01.12.2008)
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Published in Minerva chirurgica (01.12.2008)
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