Effects of an oral biodegradable device used for 12 weeks on weight reduction, cardiovascular risk factors, satiety, snacking, and meal size

Authors: Shirin, Haim, Neeland, Ian J., Ryan, Donna H., de Luis, Daniel, Lecube, Albert, Magos, Zoltan, Kenan, Yael, Amir, Ruthie, Cohen, Daniel L., Johansen, Odd Erik

Source: In Obesity Pillars December 2023 8

A Multicenter Controlled Study to Evaluate Multiple Treatments With Nonthermal Focused Ultrasound for Noninvasive Fat Reduction

Authors: Coleman, William P., Coleman, William, Weiss, Robert A., Kenkel, Jeffrey M., Ad-El, Dean D., Amir, Ruthie

Source: Dermatologic surgery. 43(1):50-57

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100173849470.0x000001&indx=1&recIds=ETOCvdc_100173849470.0x000001

Genotype-phenotype associations between chymase and angiotensin—converting enzyme gene polymorphisms in chronic systolic heart failure patients

Authors: Amir, Ruthie E., Amir, Offer, Paz, Hagar, Sagiv, Moran, Mor, Roi, Sagiv, Michael, Lewis, Basil S.

Source: In Genetics in Medicine August 2008 10(8):593-598

Aldosterone Synthase Gene Polymorphism as a Determinant of Atrial Fibrillation in Patients With Heart Failure

Authors: Amir, Offer, Amir, Ruthie E., Paz, Hagar, Mor, Roi, Sagiv, Michael, Lewis, Basil S.

Source: In The American Journal of Cardiology 2008 102(3):326-329

What Maintains the Metabolic Cost at Maximal Exercise in Heart Transplant Recipients and Coronary Artery Disease Patients?

Authors: Sagiv, Moran, Goldhammer, Ehud, Ben-Sira, David, Amir, Ruthie

Source: In Journal of Heart and Lung Transplantation 2007 26(6):617-621

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Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-Xqter.

Authors: Zhang, Wenzheng, Amir, Ruthie, Stockton, David W.

Source: American Journal of Human Genetics; April 2000, Vol. 66 Issue 4, p1461-1464, 4p

The NEDD8 Pathway Is Essential for SCFβ-TrCP-mediated Ubiquitination and Processing of the NF-κB Precursor p105

Authors: Amir, Ruthie E. ^{‡, §}, Iwai, Kazuhiro ^¶, Ciechanover, Aaron ^{‡, ‖}

Source: In Journal of Biological Chemistry 28 June 2002 277(26):23253-23259

Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms

Authors: Buyse, Inge M., Fang, Ping, Hoon, Katherine T., Amir, Ruthie E., Zoghbi, Huda Y., Roa, Benjamin B.

Source: In The American Journal of Human Genetics 2000 67(6):1428-1436

Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots

Authors: Wan, Mimi, Lee, Stephen Sung Jae, Zhang, Xianyu, Houwink-Manville, Isa, Song, Hae-Ri, Amir, Ruthie E., Budden, Sarojini, Naidu, SakkuBai, Pereira, Jose Luiz P., Lo, Ivan F.M., Zoghbi, Huda Y., Schanen, N. Carolyn, Francke, Uta

Source: In The American Journal of Human Genetics 1999 65(6):1520-1529

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Authors: Amir, Ruthie E., Van den Veyver, Ignatia B., Wan, Mimi

Source: Nature Genetics; October 1999, Vol. 23 Issue 2, p185-188, 4p

New and Advanced Picosecond Lasers for Tattoo Removal.

Authors: Adatto, Maurice A., Amir, Ruthie, Bhawalkar, Jayant, Sierra, Rafael, Bankowski, Richard, Rozen, Doran, Dierickx, Christine, Lapidoth, Moshe

Source: Current Problems in Dermatology; 2017, Vol. 52, p113-123, 11p

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