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Lerer, Israela
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1

Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with No..:

Ponger, Penina ; Kurolap, Alina ; Lerer, Israela...
Journal of Molecular Neuroscience.  72 (2022)  8 - p. 1715-1723 , 2022
Link: https://doi.org/10.1007/..
 
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2

Ultrasound findings provide clues to investigate founder mu..:

Daum, Hagit ; Lerer, Israela ; Frumkin, Ayala...
Prenatal Diagnosis.  38 (2018)  2 - p. 135-139 , 2018
Link: https://doi.org/10.1002/..
 
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3

MYORG is associated with recessive primary familial brain c..:

Arkadir, David ; Lossos, Alexander ; Rahat, Dolev...
Annals of Clinical and Translational Neurology.  6 (2018)  1 - p. 106-113 , 2018
Link: https://doi.org/10.1002/..
 
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4

The Genetics of Usher Syndrome in the Israeli and Palestini..:

Khalaileh, Ayat ; Abu-Diab, Alaa ; Ben-Yosef, Tamar...
Investigative Opthalmology & Visual Science.  59 (2018)  2 - p. 1095 , 2018
Link: https://doi.org/10.1167/..
 
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5

Features of Patients With Hereditary Mixed Polyposis Syndro..:

Lieberman, Sari ; Walsh, Tom ; Schechter, Menachem...
Gastroenterology.  152 (2017)  8 - p. 1876-1880.e1 , 2017
Link: https://doi.org/10.1053/..
 
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6

An Ashkenazi founder mutation in the PKHD1 gene:

Quint, Adina ; Sagi, Michal ; Carmi, Shai...
European Journal of Medical Genetics.  59 (2016)  2 - p. 86-90 , 2016
Link: https://doi.org/10.1016/..
 
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7

An exon trap with proper poly-A site in the GBE1 is the com..:

Akman, Orhan H. ; Kakhlon, Or ; Coku, Jorida...
Neurology.  84 (2015)  14_supplement - p. , 2015
Link: https://doi.org/10.1212/..
 
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8

Myelin-associated glycoprotein gene mutation causes Pelizae..:

Lossos, Alexander ; Elazar, Nimrod ; Lerer, Israela...
Brain.  138 (2015)  9 - p. 2521-2536 , 2015
Link: https://doi.org/10.1093/..
 
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9

Fe/S protein assembly geneIBA57mutation causes hereditary s..:

Lossos, Alexander ; Stümpfig, Claudia ; Stevanin, Giovanni...
Neurology.  84 (2015)  7 - p. 659-667 , 2015
Link: https://doi.org/10.1212/..
 
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10

Constitutional Mismatch Repair Deficiency in Israel: High P..:

Baris, Hagit N. ; Barnes-Kedar, Inbal ; Toledano, Helen...
Pediatric Blood & Cancer.  63 (2015)  3 - p. 418-427 , 2015
Link: https://doi.org/10.1002/..
 
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11

Genetic screening in patients with Retinoblastoma in Israel:

Sagi, Michal ; Frenkel, Avishag ; Eilat, Avital...
Familial Cancer.  14 (2015)  3 - p. 471-480 , 2015
Link: https://doi.org/10.1007/..
 
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12

Novel EXOSC3 mutation causes complicated hereditary spastic..:

Halevy, Ayelet ; Lerer, Israela ; Cohen, Rony...
Journal of Neurology.  261 (2014)  11 - p. 2165-2169 , 2014
Link: https://doi.org/10.1007/..
 
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13

Lynch Syndrome in high risk Ashkenazi Jews in Israel:

Goldberg, Yael ; Kedar, Inbal ; Kariiv, Revital...
Familial Cancer.  13 (2013)  1 - p. 65-73 , 2013
Link: https://doi.org/10.1007/..
 
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14

Genetic predisposition to radiation induced sarcoma: possib..:

Kadouri, Luna ; Sagi, Michal ; Goldberg, Yael...
Breast Cancer Research and Treatment.  140 (2013)  1 - p. 207-211 , 2013
Link: https://doi.org/10.1007/..
 
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15

Lipoid proteinosis with bilateral amygdalae calcifications,..:

Arkadir, David ; Lerer, Israela ; Klapholz, Laurent...
Neurology.  81 (2013)  3 - p. 303-304 , 2013
Link: https://doi.org/10.1212/..
 
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