Hakutulokset - Molho-Pessach, Vered

Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease Tekijä Ramot, Yuval, Zlotogorski, Abraham, Molho-Pessach, Vered

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Alopecia Areata and Down Syndrome: A True Association or a Coincidence Tekijä Ramot, Yuval, Molho-Pessach, Vered, Tenenbaum, Ariel, Zlotogorski, Abraham

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Multiple Nasal Papules in a 12-year-old Boy: A Quiz Tekijä ABU ASSAB, Dania, MALY, Alexander, ZLOTOGORSKI, Abraham, MOLHO-PESSACH, Vered

Hae kokoteksti Hae kokoteksti Hae kokoteksti

The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3 Tekijä Molho-Pessach, Vered, Lerer, Israela, Abeliovich, Dvorah, Agha, Ziad, Abu Libdeh, Abdulasalam, Broshtilova, Valentina, Elpeleg, Orly, Zlotogorski, Abraham

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Homozygosity Mapping Identifies a Bile Acid Biosynthetic Defect in an Adult with Cirrhosis of Unknown Etiology Tekijä Molho-Pessach, Vered, Rios, Jonathan J., Xing, Chao, Setchell, Kenneth D.R., Cohen, Jonathan C., Hobbs, Helen H.

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Accelerated coronary atherosclerosis and H syndrome Tekijä Shankarappa, Ravindranath K, Ananthakrishna, Rajiv, Math, Ravi S, Yalagudri, Sachin Dhareppa, Karur, Satish, Dwarakaprasad, Ramesh, Nanjappa, Manjunath C, Molho-Pessach, Vered

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Antibiotic Susceptibility of Cutibacterium acnes Strains Isolated from Israeli Acne Patients Tekijä SHEFFER-LEVI, Sivan, RIMON, Amit, LERER, Vanda, SHLOMOV, Tehila, COPPENHAGEN-GLAZER, Shunit, RAKOV, Chani, ZEITER, Tamara, NIR-PAZ, Ran, HAZAN, Ronen, MOLHO-PESSACH, Vered

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Chronic demodicosis in patients with immune dysregulation: An unexpected infectious manifestation of Signal transducer and activator of transcription (STAT)1 gain‐of‐function Tekijä Shamriz, Oded, Lev, Atar, Simon, Amos J, Barel, Ortal, Javasky, Elisheva, Matza‐Porges, Sigal, Shaulov, Adir, Davidovics, Zev, Toker, Ori, Somech, Raz, Zlotogorski, Abraham, Molho‐Pessach, Vered, Tal, Yuval

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Cytokine secretion and NK cell activity in human ADAM17 deficiency Tekijä Tsukerman, Pinchas, Eisenstein, Eli M., Chavkin, Maor, Schmiedel, Dominik, Wong, Eitan, Werner, Marion, Yaacov, Barak, Averbuch, Diana, Molho-Pessach, Vered, Stepensky, Polina, Kaynan, Noa, Bar-On, Yotam, Seidel, Einat, Yamin, Rachel, Sagi, Irit, Elpeleg, Orly, Mandelboim, Ofer

Hae kokoteksti Hae kokoteksti

RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1 Tekijä Abu-Libdeh, Bassam, Jhujh, Satpal S., Dhar, Srijita, Sommers, Joshua A., Datta, Arindam, Longo, Gabriel M.C., Grange, Laura J., Reynolds, John J., Cooke, Sophie L., McNee, Gavin S., Hollingworth, Robert, Woodward, Beth L., Ganesh, Anil N., Smerdon, Stephen J., Nicolae, Claudia M., Durlacher-Betzer, Karina, Molho-Pessach, Vered, Abu-Libdeh, Abdulsalam, Meiner, Vardiella, Moldovan, George-Lucian, Roukos, Vassilis, Harel, Tamar, Brosh, Robert M., Stewart, Grant S.

Hae kokoteksti Hae kokoteksti Hae kokoteksti

LGR5 expressing skin fibroblasts define a major cellular hub perturbed in scleroderma Tekijä Gur, Chamutal, Wang, Shuang-Yin, Sheban, Fadi, Zada, Mor, Li, Baoguo, Kharouf, Fadi, Peleg, Hagit, Aamar, Suhail, Yalin, Adam, Kirschenbaum, Daniel, Braun-Moscovici, Yolanda, Jaitin, Diego Adhemar, meir-salame, Tomer, Hagai, Efrat, Kragesteen, Bjørt K., Avni, Batia, Grisariu, Sigal, Bornstein, Chamutal, Shlomi-Loubaton, Shir, David, Eyal, Shreberk-Hassidim, Rony, Molho-Pessach, Vered, Amar, Dalit, Tzur, Tomer, Kuint, Rottem, Gross, Moshe, Barboy, Oren, Moshe, Adi, Fellus-Alyagor, Liat, Hirsch, Dana, Addadi, Yoseph, Erenfeld, Shlomit, Biton, Moshe, Tzemach, Tehila, Elazary, Anat, Naparstek, Yaakov, Tzemach, Reut, Weiner, Assaf, Giladi, Amir, Balbir-Gurman, Alexandra, Amit, Ido

Hae kokoteksti Hae kokoteksti Hae kokoteksti