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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

Normal and abnormal fetal brain development during the third trimester as demonstrated by neurosonography

G. Malinger, D. Lev, T. Lerman-Sagie

Journal:

European Journal of Radiology

Year:

2006

Language:

english

File:

PDF, 1.26 MB

english, 2006

4

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

5

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

6

P24.07: Posterior fossa imaging features enabling diagnosis of PHACE syndrome in utero

Leibovitz, Z., Haratz, K.K., Gindes, L., Tamarkin, M., Bakry, H., Weizman, B., Shapiro, I., Sagie, S., Malinger, G., Ben-Sira, L., Lev, D., Lerman-Sagie, T.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2017

Language:

english

File:

PDF, 57 KB

english, 2017

7

Fetal Neurology

Malinger, Gustavo, Lerman-Sagie, Tally

Journal:

European Journal of Paediatric Neurology

Year:

2018

Language:

english

File:

PDF, 260 KB

english, 2018

8

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

9

The fetal cerebellar vermis: normal development as shown by transvaginal ultrasound

G. Malinger, S. Ginath, T. Lerman-Sagie, N. Watemberg, D. Lev, M. Glezerman

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 193 KB

english, 2001

10

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

11

Non-visualization of the cavum septi pellucidi is not synonymous with agenesis of the corpus callosum

G. Malinger, D. Lev, M. Oren, T. Lerman-Sagie

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2012

Language:

english

File:

PDF, 420 KB

english, 2012

12

Differential diagnosis in fetuses with absent septum pellucidum

G. Malinger, D. Lev, D. Kidron, F. Heredia, R. Hershkovitz, T. Lerman-Sagie

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2005

Language:

english

File:

PDF, 387 KB

english, 2005

13

Three-dimensional sagittal reconstruction of the corpus callosum: fact or artifact?

G. Malinger, T. Lerman-Sagie, F. Viñals

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2006

Language:

english

File:

PDF, 131 KB

english, 2006

14

Is fetal magnetic resonance imaging superior to neurosonography for detection of brain anomalies?

G. Malinger, D. Lev, T. Lerman-Sagie

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2002

Language:

english

File:

PDF, 5.54 MB

english, 2002

15

Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene

E. Leshinsky-Silver, D. Lev, Z. Tzofi-Berman, S. Cohen, A. Saada, M. Yanoov-Sharav, E. Gilad, T. Lerman-Sagie

Journal:

Biochemical and Biophysical Research Communications

Year:

2005

Language:

english

File:

PDF, 433 KB

english, 2005

16

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

17

Does Physical Therapy Improve Outcome in Infants with Joint Hypermobility and Benign Hypotonia?

Mintz-Itkin, R., Lerman-Sagie, T., Zuk, L., Itkin-Webman, T., Davidovitch, M.

Journal:

Journal of Child Neurology

Year:

2009

Language:

english

File:

PDF, 165 KB

english, 2009

18

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

19

Significance of Microcephaly Among Children With Developmental Disabilities

Watemberg, N., Silver, S., Harel, S., Lerman-Sagie, T.

Journal:

Journal of Child Neurology

Year:

2002

Language:

english

File:

PDF, 617 KB

english, 2002

20

Should Autistic Children Be Evaluated for Mitochondrial Disorders?

Lerman-Sagie, T., Leshinsky-Silver, E., Watemberg, N., Lev, D.

Journal:

Journal of Child Neurology

Year:

2004

Language:

english

File:

PDF, 342 KB

english, 2004

21

Prenatal Brain Disruption in Molybdenum Cofactor Deficiency

Carmi-Nawi, N., Malinger, G., Mandel, H., Ichida, K., Lerman-Sagie, T., Lev, D.

Journal:

Journal of Child Neurology

Year:

2011

Language:

english

File:

PDF, 402 KB

english, 2011

22

Congenital Ataxia, Mental Retardation, and Dyskinesia Associated With a Novel CACNA1A Mutation

Blumkin, L., Michelson, M., Leshinsky-Silver, E., Kivity, S., Lev, D., Lerman-Sagie, T.

Journal:

Journal of Child Neurology

Year:

2010

Language:

english

File:

PDF, 184 KB

english, 2010

23

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

24

CBD-enriched medical cannabis for intractable pediatric epilepsy. The current Israeli experience

Tzadok, Michal, Uliel-Siboni, Shimrit, Linder, Ilan, Kramer, Uri, Epstein, Orna, Menascu, Shai, Nissenkorn, Andrea, Yosef, Omer Bar, Hyman, Eli, Granot, Dorit, Dor, Michael, Lerman-Sagie, Tali, Ben-Ze

Journal:

Year:

2016

Language:

english

File:

PDF, 189 KB

english, 2016

25

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

26

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

27

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

28

EP03.07: Prenatal diagnosis of 22q11.2 microdeletion: minor cardiac finding detected in mid-trimester scan associated with severe bilateral perisylvian polymicrogyria in late gestation

Weizman, B., Bakry, H., Haratz, K.K., Gindes, L., Tamarkin, M., Sagie, S., Shapiro, I., Cohen, G., Ben-Sira, L., Lev, D., Lerman-Sagie, T., Leibovitz, Z.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2017

Language:

english

File:

PDF, 40 KB

english, 2017

29

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

30

Heterogeneity in adducted thumbs sequence

Moldavsky, M., Lerman-Sagie, T., Kutai, M., Legum, C., Harel, S.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 244 KB

english, 1997

31

Glycogen storage disease type 1a in Israel: Biochemical, clinical, and mutational studies

Parvari, Ruti, Lei, Ke-Jian, Bashan, Nava, Hershkovitz, Eli, Korman, Stanley H., Barash, Varda, Lerman-Sagie, Tali, Mandel, Hannah, Chou, Janice Yang, Moses, Shimon W.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 143 KB

english, 1997

32

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

33

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

34

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

35

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

36

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

37

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

38

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

39

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

40

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

41

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

42

The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings

RS Devon, JR Helm, GA Rouleau, Y Leitner, T Lerman-Sagie, D Lev, MR Hayden

Journal:

Clinical Genetics

Year:

2003

Language:

english

File:

PDF, 777 KB

english, 2003

43

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

44

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

45

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

46

Prenatal brain imaging in congenital toxoplasmosis

G. Malinger, H. Werner, J. C. Rodriguez Leonel, M. Rebolledo, M. Duque, S. Mizyrycki, T. Lerman-Sagie, M. Herrera

Journal:

Prenatal Diagnosis

Year:

2011

Language:

english

File:

PDF, 255 KB

english, 2011

47

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

48

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

49

Case report 416

Tally Lerman-Sagie, Michael Grunebaum, Marc Mimouni

Journal:

Skeletal Radiology

Year:

1987

Language:

english

File:

PDF, 1.16 MB

english, 1987

50

CSF glucose levels in febrile infants

T. Lerman-Sagie, M. Shohat, M. Nitzan

Journal:

European Journal of Pediatrics

Year:

1988

Language:

english

File:

PDF, 155 KB

english, 1988