검색어 : 통합검색[Weisz Rachel]
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41
- Homozygous MED25 mutation implicated in eye-intellectual disability syndrome
- Basel-Vanagaite, Lina; Smirin-Yosef, Pola; Essakow, Jenna Lee; Tzur, Shay; Lagovsky, Irina; Maya, Idit; Pasmanik-Chor, Metsada; Yeheskel, Adva; Konen, Osnat; Orenstein, Naama; Weisz Hubshman, Monika; Drasinover, Valerie; Magal, Nurit; Peretz Amit, Gaby; Zalzstein, Yael; Zeharia, Avraham; Shohat, Mordechai; Straussberg, Rachel; Monté , Didier; Salmon-Divon, Mali; Behar, Doron M.; ; (Human genetics, v.134, 2015, pp.577-587)
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42
- Application of the Movement Disorder Society prodromal criteria in healthy <i>G2019S</i>‐<i>LRRK2</i> carriers
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Mirelman, Anat;
Saunders‐
Pullman, Rachel;
Alcalay, Roy N.;
Shustak, Shiran;
Thaler, Avner;
Gurevich, Tanya;
Raymond, Deborah;
Mejia‐
Santana, Helen;
Orbe Reilly, Martha;
Ozelius, Laurie;
Clark, Lorraine;
Gana‐
Weisz, Mali;
Bar‐
Shira, Anat;
Orr‐
Utreger, Avi;
Bressman, Susan B.;
Marder, Karen;
Giladi, Nir;
Movement Disorders Unit, Neurological Institute, Tel Aviv Medical Center, Tel‐
Aviv, Israel;
Departments of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA;
Department of Neurology, College of Physicians and Surgeons, Taub Institute for Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, USA;
Movement Disorders Unit, Neurological Institute, Tel Aviv Medical Center, Tel‐
Aviv, Israel;
Movement Disorders Unit, Neurological Institute, Tel Aviv Medical Center, Tel‐
Aviv, Israel;
Movement Disorders Unit, Neurological Institute, Tel Aviv Medical Center, Tel‐
Aviv, Israel;
Departments of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA
- Mirelman, Anat; Bernad‐ Elazari, Hagar; Thaler, Avner; Giladi‐ Yacobi, Eytan; Gurevich, Tanya; Gana‐ Weisz, Mali; Saunders‐ Pullman, Rachel; Raymond, Deborah; Doan, Nancy; Bressman, Susan B.; Marder, Karen S.; Alcalay, Roy N.; Rao, Ashwini K.; Berg, Daniela; Brockmann, Kathrin; Aasly, Jan; Waro, Bjørg Johanne; Tolosa, Eduardo; Vilas, Dolores; Pont‐ Sunyer, Claustre; Orr‐ Urtreger, Avi; Hausdorff, Jeffrey M.; Giladi, Nir; Laboratory for Early Markers of Neurodegeneration, Tel Aviv Medical Center, Tel Aviv, Israel; Laboratory for Early Markers of Neurodegeneration, Tel Aviv Medical Center, Tel Aviv, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Genetic Institute, Tel Aviv Medical Center, Tel Aviv, Israel; Departments of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA; Departments of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA; Departments of Neurology, Mount Sinai Beth Israel Med; (Movement disorders : official journal of the Movement Disorder Society, v.31, 2016, pp.1527-1534)
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50
- Carbon and Iron Deficiencies in Quiescent Galaxies at z = 1–3 from JWST-SUSPENSE: Implications for the Formation Histories of Massive Galaxies
- Aliza G. Beverage; Martje Slob; Mariska Kriek; Charlie Conroy; Guillermo Barro; Rachel Bezanson; Gabriel Brammer; Chloe M. Cheng; Anna de Graaff; Natascha M. Förster Schreiber; Marijn Franx; Brian Lorenz; Pavel E. Mancera Piña; Danilo Marchesini; Adam Muzzin; Andrew B. Newman; Sedona H. Price; Alice E. Shapley; Mauro Stefanon; Katherine A. Suess; Pieter van Dokkum; David Weinberg; Daniel R. Weisz; ; (The Astrophysical Journal, v., 2025, )
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