Canlyniadau Chwilio - Tally Lerman‐Sagie
- Dangos 1 - 20 canlyniadau o 35
- Ewch i'r Dudalen Nesaf
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The fetal cerebellum. Pitfalls in diagnosis and management gan G. Malinger, Dorit Lev, Tally Lerman‐Sagie
Cyhoeddwyd 2009Revisão -
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Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome gan F. D’Antonio, Athar Khalil, Cathérine Garel, G. Pilu, Giuseppe Rizzo, Tally Lerman‐Sagie, A. Bhide, B. Thilaganathan, Lamberto Manzoli, Aris T. Papageorghiou
Cyhoeddwyd 2015Revisão -
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Systematic review and meta‐analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies gan F. D’Antonio, A. Khalil, Cathérine Garel, G. Pilu, Giuseppe Rizzo, Tally Lerman‐Sagie, A. Bhide, B. Thilaganathan, Lamberto Manzoli, Aris T. Papageorghiou
Cyhoeddwyd 2015Revisão -
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Effect of cyclic, low dose pyrimethamine treatment in patients with Late Onset Tay Sachs: an open label, extended pilot study gan Etty Osher, Aviva Fattal‐Valevski, Liora Sagie, Nataly Urshanski, Nadav Sagiv, Leah Peleg, Tally Lerman‐Sagie, Ari Zimran, Deborah Elstein, Ruth Navon, Avi Valevski, Naftali Stern
Cyhoeddwyd 2015Artigo -
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Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abn... gan Ghayda Mirzaa, Robert L. Conway, Karen W. Gripp, Tally Lerman‐Sagie, Dawn H. Siegel, Linda S. deVries, Dorit Lev, Nancy Kramer, Elizabeth Hopkins, John M. Graham, William B. Dobyns
Cyhoeddwyd 2012Artigo -
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White matter abnormalities and dystonic motor disorder associated with mutations in the <i>SLC16A2</i> gene gan Artemis Gika, Ata Siddiqui, Anthony Hulse, SELVAKUMARI EDWARD, Penny Fallon, Meriel E. McEntagart, Wajanat Jan, Dragana Josifova, TALLY LERMAN‐SAGIE, James Drummond, Edward D. Thompson, Samuel Refetoff, Carsten G. Bönnemann, Heinz Jungbluth
Cyhoeddwyd 2009Artigo -
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Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy gan Orly Agamy, Bruria Ben Zeev, Dorit Lev, Barak Marcus, Dina Fine, Dan Su, Ginat Narkis, Rivka Ofir, Chen Hoffmann, Esther Leshinsky‐Silver, Hagit Flusser, Sara Sivan, Dieter Söll, Tally Lerman‐Sagie, Ohad S. Birk
Cyhoeddwyd 2010Artigo -
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Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis? gan Z. Leibovitz, Etty Daniel‐Spiegel, G. Malinger, Karina Krajden Haratz, M. Tamarkin, L. Gindes, Letizia Schreiber, Liat Ben‐Sira, Dorit Lev, I. Shapiro, H. Bakry, B. Weizman, A. Zreik, S. Egenburg, Ayala Arad, R. Tepper, Debora Kidron, Tally Lerman‐Sagie
Cyhoeddwyd 2015Artigo -
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<i><scp>GRIN</scp>1</i> mutations cause encephalopathy with infantile‐onset epilepsy, and hyperkinetic and stereotyped movement disorders gan Chihiro Ohba, Masaaki Shiina, Jun Tohyama, Kazuhiro Haginoya, Tally Lerman‐Sagie, Nobuhiko Okamoto, Lubov Blumkin, Dorit Lev, Souichi Mukaida, Fumihito Nozaki, Mitsugu Uematsu, Akira Onuma, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Fumiaki Tanaka, Mitsuhiro Kato, Kazuhiro Ogata, Hirotomo Saitsu, Naomichi Matsumoto
Cyhoeddwyd 2015Artigo -
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Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus gan Robyn H. Wallace, Ingrid E. Scheffer, Shaun Barnett, M. Richards, Leanne M. Dibbens, R. Desai, Tally Lerman‐Sagie, Dorit Lev, Aziz Mazarib, Nathan Brand, Bruria Ben‐Zeev, Igor Goikhman, Rita Singh, Gabriel Kremmidiotis, Alison Gardner, G.R. Sutherland, Alfred L. George, John C. Mulley, Samuel F. Berkovic
Cyhoeddwyd 2001Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Genetics
Medicine
Gene
Fetus
Pregnancy
Epilepsy
Neuroscience
Pathology
Radiology
Anatomy
Pediatrics
Internal medicine
Psychiatry
Mutation
Missense mutation
Biochemistry
Magnetic resonance imaging
Microcephaly
Polymicrogyria
Prenatal diagnosis
Psychology
Ventriculomegaly
Gestational age
Lissencephaly
Phenotype
Ultrasound
Cohort
Copy-number variation
Genome