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1

Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis

Ghayda M. 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 Jr, William B. Dobyns

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 1.32 MB

english, 2012

2

Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromes

Karen W. Gripp, Elizabeth Hopkins, Chana Vinkler, Dorit Lev, Gustavo Malinger, Tally Lerman-Sagie, William B. Dobyns

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 412 KB

english, 2009

3

Mortality in Dravet syndrome

Cooper, Monica S., Mcintosh, Anne, Crompton, Douglas E., McMahon, Jacinta M., Schneider, Amy, Farrell, Kevin, Ganesan, Vijeya, Gill, Deepak, Kivity, Sara, Lerman-Sagie, Tally, McLellan, Ailsa, Pelekan

Journal:

Epilepsy Research

Year:

2016

Language:

english

File:

PDF, 425 KB

english, 2016

4

Malformations of Cortical Development: From Postnatal to Fetal Imaging

Lerman-Sagie, Tally, Leibovitz, Zvi

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2016

File:

PDF, 846 KB

2016

5

Fetal Neurology

Malinger, Gustavo, Lerman-Sagie, Tally

Journal:

European Journal of Paediatric Neurology

Year:

2018

Language:

english

File:

PDF, 260 KB

english, 2018

6

The subarachnoid space: normal fetal development as demonstrated by transvaginal ultrasound

Gustavo Malinger, Tally Lerman-Sagie, Reuwen Achiron, Shlomo Lipitz

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 154 KB

english, 2000

7

Adding Video Recording Increases the Diagnostic Yield of Routine Electroencephalograms in Children with Frequent Paroxysmal Events

Nathan Watemberg, Barak Tziperman, Ron Dabby, Mariana Hasan, Liora Zehavi, Tally Lerman-Sagie

Journal:

Year:

2005

Language:

english

File:

PDF, 53 KB

english, 2005

8

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin

Ingrid Tein, Orly Elpeleg, Bruria Ben-Zeev, Stanley H. Korman, Alexander Lossos, Dorit Lev, Tally Lerman-Sagie, Esther Leshinsky-Silver, Jerry Vockley, Gerard T. Berry, Anne-Marie Lamhonwah, Dietrich

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 177 KB

english, 2008

9

Behavioral Phenotypes of Genetic Syndromes: A Reference Guide for Psychiatrists

MOLDAVSKY, MARIA, LEV, DORIT, LERMAN-SAGIE, TALLY, D, M.K.

Journal:

Journal of the American Academy of Child & Adolescent Psychiatry

Year:

2001

Language:

english

File:

PDF, 154 KB

english, 2001

10

Effect of cyclic, low dose pyrimethamine treatment in patients with Late Onset Tay Sachs: an open label, extended pilot study

Osher, Etty, Fattal-Valevski, Aviva, Sagie, Liora, Urshanski, Nataly, Sagiv, Nadav, Peleg, Leah, Lerman-Sagie, Tally, Zimran, Ari, Elstein, Deborah, Navon, Ruth, Valevski, Avi, Stern, Naftali

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 629 KB

english, 2015

11

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population

Tein, Ingrid, Elpeleg, Orly, Ben-Zeev, Bruria, Korman, Stanley H., Lossos, Alexander, Lev, Dorit, Lerman-Sagie, Tally, Vockley, Gerard, Berry, Gerard T., Lamhownah, Anne-Marie, Matern, Dieter, Roe, Ch

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 15 KB

english, 2007

12

GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders

Ohba, Chihiro, Shiina, Masaaki, Tohyama, Jun, Haginoya, Kazuhiro, Lerman-Sagie, Tally, Okamoto, Nobuhiko, Blumkin, Lubov, Lev, Dorit, Mukaida, Souichi, Nozaki, Fumihito, Uematsu, Mitsugu, Onuma, Akira

Journal:

Year:

2015

Language:

english

File:

PDF, 1.29 MB

english, 2015

13

Technetium 99m Ethylcysteinate Dimer Single-Photon Emission Computed Tomography (SPECT) During Intellectual Stress Test in Children and Adolescents With Pure Versus Comorbid Attention-Deficit Hyperactivity Disorder (ADHD)

Lorberboym, Mordechai, Watemberg, Nathan, Nissenkorn, Andreea, Nir, Batia, Lerman-Sagie, Tally

Journal:

Journal of Child Neurology

Year:

2004

Language:

english

File:

PDF, 584 KB

english, 2004

14

Diagnostic approach to fetal microcephaly

Leibovitz, Zvi, Lerman-Sagie, Tally

Journal:

European Journal of Paediatric Neurology

Year:

2018

Language:

english

File:

PDF, 1.26 MB

english, 2018

15

Neurological involvement in a child with the wrinkly skin syndrome

Azuri, Joseph, Mizrachi, Avraham, Weintraub, Shlomo, Lerman-Sagie, Tally

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 223 KB

english, 1999

16

Syndrome of osteopetrosis and muscular degeneration associated with cerebro-oculo-facio-skeletal changes

Dr. Tally Lerman-Sagie, Yael Levi, Deborah Kidron, Michael Grünebaum, Menachem Nitzan, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 386 KB

english, 1987

17

New findings in a patient with dubowitz syndrome: Velopharyngeal insufficiency and hypoparathyroidism

Tally Lerman-Sagie, Paul Merlob, Avinoam Shuper, Rivka Kauli, Zilli Kozokaro, Michael Grunebaum, Marc Mimouni

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 267 KB

english, 1990

18

A new autosomal recessive syndrome with Zellweger-like manifestations

Joe K. Ahn, Dorit Lev, Esther Leshinsky-Silver, Mira Ginzberg, Tally Lerman-Sagie

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 138 KB

english, 2003

19

Familial optic atrophy with white matter changes

Chana Vinkler, Dorit Lev, Hadas Kalish, Nathan Watemberg, Miri Yanoov-Sharav, Esther Leshinsky-Silver, Tally Lerman-Sagie

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 107 KB

english, 2003

20

A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms

Dorit Lev, Yuval Weigl, Mariana Hasan, Eva Gak, Michael Davidovich, Chana Vinkler, Esther Leshinsky-Silver, Tally Lerman-Sagie, Nathan Watemberg

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 207 KB

english, 2007

21

Mosaic marker chromosome 16 resulting in 16q11.2–q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasia

Ayelet Zerem, Chana Vinkler, Marina Michelson, Esther Leshinsky-Silver, Tally Lerman-Sagie, Dorit Lev

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 2.14 MB

english, 2011

22

Rare copy number variants are an important cause of epileptic encephalopathies

Heather C. Mefford, Simone C. Yendle, Cynthia Hsu, Joseph Cook, Eileen Geraghty, Jacinta M. McMahon, Orvar Eeg-Olofsson, Lynette G. Sadleir, Deepak Gill, Bruria Ben-Zeev, Tally Lerman-Sagie, Mark Mack

Journal:

Annals of Neurology

Year:

2011

Language:

english

File:

PDF, 879 KB

english, 2011

23

Hypomyelinating leukoencephalopathy with paroxysmal tonic upgaze and absence of psychomotor development

Lubov Blumkin, Dorit Lev, Nathan Watemberg, Tally Lerman-Sagie

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 98 KB

english, 2007

24

Autoimmune epilepsy: Distinct subpopulations of epilepsy patients harbor serum autoantibodies to either glutamate/AMPA receptor GluR3, glutamate/NMDA receptor subunit NR2A or double-stranded DNA

Yonatan Ganor, Hadassa Goldberg-Stern, Tally Lerman-Sagie, Vivian I. Teichberg, Mia Levite

Journal:

Epilepsy Research

Year:

2005

Language:

english

File:

PDF, 497 KB

english, 2005

25

Absence Seizures Aggravated by Valproic Acid

Tally Lerman-Sagie, Nathan Watemberg, Uri Kramer, Eli Shahar, Pinchas Lerman

Journal:

Year:

2001

Language:

english

File:

PDF, 28 KB

english, 2001

26

The fetal cerebellum. Pitfalls in diagnosis and management

Gustavo Malinger, Dorit Lev, Tally Lerman-Sagie

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 323 KB

english, 2009

27

Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?

Natalie Farkas, Chen Hoffmann, Liat Ben-Sira, Dorit Lev, Avraham Schweiger, Dvora Kidron, Tally Lerman-Sagie, Gustavo Malinger

Journal:

Prenatal Diagnosis

Year:

2011

Language:

english

File:

PDF, 146 KB

english, 2011

28

Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNA

Esther Leshinsky-Silver, Michal Perach, Erena Basilevsky, Eli Hershkovitz, Miri Yanoov-Sharav, Tally Lerman-Sagie, Dorit Lev

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 69 KB

english, 2003

29

Adverse reactions of Topiramate and Lamotrigine in children

Tamar Shechter, Zamir Shorer, Uri Kramer, Tally Lerman-Sagie, Elisheva Ronen, Rimona Rotem, Rafael Gorodischer

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2005

Language:

english

File:

PDF, 73 KB

english, 2005

30

Case report 416

Tally Lerman-Sagie, Michael Grunebaum, Marc Mimouni

Journal:

Skeletal Radiology

Year:

1987

Language:

english

File:

PDF, 1.16 MB

english, 1987

31

A prospective, multicenter, open-label assessment of atomoxetine in non-North American children and adolescents with ADHD

Jan K. Buitelaar, Marina Danckaerts, Christopher Gillberg, Alessandro Zuddas, Katja Becker, Manuel Bouvard, Jenny Fagan, Julia Gadoros, Valerie Harpin, Philip Hazell, Mats Johnson, Tally Lerman-Sagie,

Journal:

European Child & Adolescent Psychiatry

Year:

2004

Language:

english

File:

PDF, 206 KB

english, 2004

32

Sulthiame in childhood epilepsy

Bruria Ben-Zeev, Nathan Watemberg, Pinchas Lerman, Itshak Barash, Nathan Brand, Tally Lerman-Sagie

Journal:

Pediatrics International

Year:

2004

Language:

english

File:

PDF, 74 KB

english, 2004

33

Developmental coordination disorder in children with attention-deficit–hyperactivity disorder and physical therapy intervention

Nathan Watemberg, Nilly Waiserberg, Luba Zuk, Tally Lerman-Sagie

Journal:

Developmental Medicine & Child Neurology

Year:

2007

Language:

english

File:

PDF, 186 KB

english, 2007

34

White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene

ARTEMIS D GIKA, ATA SIDDIQUI, ANTHONY J HULSE, SELVAKUMARI EDWARD, PENNY FALLON, MERIEL E MCENTAGART, WAJANAT JAN, DRAGANA JOSIFOVA, TALLY LERMAN-SAGIE, JAMES DRUMMOND, EDWARD THOMPSON, SAMUEL REFETOF

Journal:

Developmental Medicine & Child Neurology

Year:

2010

Language:

english

File:

PDF, 699 KB

english, 2010

35

Clinical Correlates of Occipital Intermittent Rhythmic Delta Activity (OIRDA) in Children

Nathan Watemberg, Ilan Linder, Ron Dabby, Lubov Blumkin, Tally Lerman-Sagie

Journal:

Year:

2007

Language:

english

File:

PDF, 135 KB

english, 2007

36

Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation

Cristina Gomez-Abad, Zaid Afawi, Amos D. Korczyn, Adel Misk, Stavit A. Shalev, Ronen Spiegel, Tally Lerman-Sagie, Dorit Lev, Katherine L. Kron, Pilar Gómez-Garre, Jose M. Serratosa, Samuel F. Berkovic

Journal:

Year:

2007

Language:

english

File:

PDF, 110 KB

english, 2007

37

Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?

Angelique E. J. Sijben, Pasiri Sithinamsuwan, Ashalata Radhakrishnan, Radwa A. B. Badawy, Leanne Dibbens, Aziz Mazarib, Dorit Lev, Tally Lerman-Sagie, Rachel Straussberg, Samuel F. Berkovic, Ingrid E.

Journal:

Year:

2009

Language:

english

File:

PDF, 121 KB

english, 2009

38

Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region

Marina Michelson, Anat Ben-Sasson, Chana Vinkler, Esther Leshinsky-Silver, Ifat Netzer, Ayala Frumkin, Sara Kivity, Tally Lerman-Sagie, Dorit Lev

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 329 KB

english, 2012

39

Mutation in theAP4B1gene cause hereditary spastic paraplegia type 47 (SPG47)

Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, Nina Schlipf, Christopher Schröder, Julia Schicks, Dorit Lev, Olaf Riess, Tally Lerman-Sagie, Ludger Schöls

Journal:

Year:

2012

Language:

english

File:

PDF, 184 KB

english, 2012

40

Genetic Counseling and Testing for FSHD (Facioscapulohumeral Muscular Dystrophy) in the Israeli Population

Yanoov-Sharav, Miri, Leshinsky-Silver, Esther, Cohen, Sarit, Vinkler, Chana, Michelson, Marina, Lerman-Sagie, Tally, Ginzberg, Mira, Sadeh, Menahem, Lev, Dorit

Journal:

Journal of Genetic Counseling

Year:

2012

Language:

english

File:

PDF, 210 KB

english, 2012

41

Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy

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, O

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.26 MB

english, 2010

42

Comparison between neurosonography and MRI in the evaluation of fetal CNS pathologies – A blinded study

Zahi Ben-Aroya, Liat Ben-Sira, Dorit Lev, Tally Lerman-Sagie, Gustavo Malinger

Journal:

American Journal of Obstetrics and Gynecology

Year:

2005

Language:

english

File:

PDF, 90 KB

english, 2005

43

Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosis

Gustavo Malinger, Neriman Zahalka, Dvora Kidron, Liat Ben-Sira, Dorit Lev, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2006

Language:

english

File:

PDF, 160 KB

english, 2006

44

A benign congenital myopathy in an inbred Samaritan family

Dorit Lev, Menachem Sadeh, Nathan Watemberg, Ron Dabby, Chana Vinkler, Mira Ginzberg, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2006

Language:

english

File:

PDF, 329 KB

english, 2006

45

Letter to the editor

Dorit Lev, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 151 KB

english, 2007

46

Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration—A late onset variant of PCH-1?

Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, Lubov Blumkin, Stavit A. Shalev, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2008

Language:

english

File:

PDF, 667 KB

english, 2008

47

Letter to the Editor

Tally Lerman-Sagie, Dorit Lev

Journal:

European Journal of Paediatric Neurology

Year:

2009

Language:

english

File:

PDF, 69 KB

english, 2009

48

Familial leukoencephalopathy with slowly progressive dystonia and ataxia

Lubov Blumkin, Hanna Mandel, Marieta Anca-Herschkovitsch, Sara Kivity, Dorit Lev, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2009

Language:

english

File:

PDF, 276 KB

english, 2009

49

Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation

Daniella Nishri, Lubov Blumkin, Dorit Lev, Esther Leshinsky-Silver, Mohammad Abu-Rashid, Rachael Birch, Sameer M. Zuberi, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2010

Language:

english

File:

PDF, 121 KB

english, 2010

50

Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother

Marina Michelson, Avi Eden, Chana Vinkler, Esther Leshinsky-Silver, Uri Kremer, Tally Lerman-Sagie, Dorit Lev

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 183 KB

english, 2011

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