日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Integrating mind and body: Investigating differential activation of nodes of the default mode network

整合身心:探究默认模式网络节点的差异性激活

Linchevski, Inbal; Maimon, Amber; Golland, Yulia; Zeharia, Noa; Amedi, Amir; Levit-Binnun, Nava

Elevated Alpha-Fetoprotein in Infantile-Onset Niemann-Pick Type C Disease with Liver Involvement

婴儿期发病的尼曼-匹克C型病伴肝脏受累患者的甲胎蛋白升高

Kraus, Dror; Abdelrahim, Huda; Waisbourd-Zinman, Orith; Domin, Elena; Zeharia, Avraham; Staretz-Chacham, Orna

Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects

以色列九个家族和德国两例散发病例中的经典型黄嘌呤尿症:分子、生化和群体遗传学方面

Peretz, Hava; Lagziel, Ayala; Bittner, Florian; Kabha, Mustafa; Shtauber-Naamati, Meirav; Zhuravel, Vicki; Usher, Sali; Rump, Steffen; Wollers, Silke; Bork, Bettina; Mandel, Hanna; Falik-Zaccai, Tzipora; Kalfon, Limor; Graessler, Juergen; Zeharia, Avraham; Heib, Nasser; Shalev, Hannah; Landau, Daniel; Levartovsky, David

Symptoms and clinical parameters of pediatric and adolescent migraine, by gender - a retrospective cohort study

按性别划分的儿童和青少年偏头痛的症状和临床参数——一项回顾性队列研究

Eidlitz-Markus, Tal; Zeharia, Avraham

Mitochondrial hepato-encephalopathy due to deficiency of QIL1/MIC13 (C19orf70), a MICOS complex subunit

由于 QIL1/MIC13(C19orf70)缺乏(MICOS 复合亚基)导致的线粒体肝性脑病

Avraham Zeharia, Jonathan R Friedman, Ana Tobar, Ann Saada, Osnat Konen, Yacov Fellig, Avraham Shaag, Jodi Nunnari, Orly Elpeleg

Sustained Release of Antibacterial Lipopeptides from Biodegradable Polymers against Oral Pathogens

从可生物降解聚合物中持续释放抗菌脂肽对抗口腔病原体

Eckhard, Lea H; Houri-Haddad, Yael; Sol, Asaf; Zeharia, Rotem; Shai, Yechiel; Beyth, Shaul; Domb, Abraham J; Bachrach, Gilad; Beyth, Nurit

Phenotypic variability in patients with fanconi-bickel syndrome with identical mutations

具有相同突变的范科尼-比克尔综合征患者的表型变异性

Fridman, Elena; Zeharia, Avraham; Markus-Eidlitz, Tal; Haimi Cohen, Yishai

EHMTI-0112. Association of age at onset of migraine with family history of migraine in children attending a pediatric headache clinic

EHMTI-0112. 偏头痛发作年龄与儿童偏头痛家族史的相关性研究(儿科头痛门诊就诊儿童)

Defrin, Ruth; Riabinin, Miri; Feingold, Yelena; Schreiber, Shaul; Pick, Chaim G; Markus, T Eidlitz; Haimi-Cohen, Y; Zeharia, A; Markus, TAL Eidlitz

Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1

由编码甘油-3-磷酸脱氢酶1的GPD1基因突变引起的短暂性婴儿高甘油三酯血症、脂肪肝和肝纤维化

Basel-Vanagaite, Lina; Zevit, Noam; Har Zahav, Adi; Guo, Liang; Parathath, Saj; Pasmanik-Chor, Metsada; McIntyre, Adam D; Wang, Jian; Albin-Kaplanski, Adi; Hartman, Corina; Marom, Daphna; Zeharia, Avraham; Badir, Abir; Shoerman, Oded; Simon, Amos J; Rechavi, Gideon; Shohat, Mordechai; Hegele, Robert A; Fisher, Edward A; Shamir, Raanan

Toward genotype phenotype correlations in GFM1 mutations

GFM1 突变中的基因型与表型相关性

Louise Galmiche, Valérie Serre, Marine Beinat, Raïssa Zossou, Zahra Assouline, Anne-Sophie Lebre, Florence Chretien, Ruthie Shenhav, Avraham Zeharia, Ann Saada, Vanessa Vedrenne, Nathalie Boddaert, Pascale de Lonlay, Marlène Rio, Arnold Munnich, Agnès Rötig