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Characteristics of genetic diseases in consanguineous populations in the genomic era: Lessons from Arab communities in North Israel

Clinical genetics, 2019-01, Vol.95 (1), p.3-9

Shalev, S.A.

2019

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Expanding the genotypic spectrum of Perrault syndrome

Clinical genetics, 2017-02, Vol.91 (2), p.302-312

2017

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Desert flash floods form hyperpycnal flows in the coral-rich Gulf of Aqaba, Red Sea

Earth and planetary science letters, 2015-05, Vol.417, p.87-98

2015

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Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family

The Journal of infection, 2023-10, Vol.87 (4), p.336-338

2023

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A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Clinical genetics, 2016-05, Vol.89 (5), p.603-607

2016

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Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects

British journal of dermatology (1951), 2016-03, Vol.174 (3), p.562-568

2016

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Erratum to “A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery” [Int. J. Obstetric Anesth. 49 (2022) 103229]

International journal of obstetric anesthesia, 2023-11, Vol.56, p.103903-103903, Article 103903

2023

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DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation

Clinical genetics, 2016-06, Vol.89 (6), p.724-727

2016

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Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small‐platelet thrombocytopenia

Journal of thrombosis and haemostasis, 2015-07, Vol.13 (7), p.1285-1292

2015

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Obstetric quality of recovery scoring tool: assessment of validity, reliability and feasibility in an Israeli cesarean delivery population

International journal of obstetric anesthesia, 2020-11, Vol.44, p.51-51

2020

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A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery

International journal of obstetric anesthesia, 2022-02, Vol.49, p.103229-103229, Article 103229

2022

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THU0222 The Diagnosis of Familial Mediterranean Fever Following The Initial Presentation of Monoarthritis

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.268-269

2016

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Distinguishability between ancient and modern leaded tin bronzes by the composition of their lead inclusions

Science and technology of archaeological research, 2019-12, Vol.5 (2), p.29-35

2019

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Developmental Dyscalculia

Journal of child neurology, 2004-10, Vol.19 (10), p.765-771

Shalev, Ruth S.

2004

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Severe infantile male encephalopathy is a result of early post-zygotic WDR45 somatic mutation

Clinical genetics, 2016-12, Vol.90 (6), p.560-562

2016

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Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10

British journal of dermatology (1951), 2015-07, Vol.173 (1), p.293-296

2015

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Developmental dyscalculia: a prospective six-year follow-up

Developmental medicine and child neurology, 2005-02, Vol.47 (2), p.121-125

2005

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Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans

Journal of medical genetics, 2010-08, Vol.47 (8), p.533-537

2010

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Lightning flash multiplicity in eastern Mediterranean thunderstorms

Natural hazards and earth system sciences, 2014-02, Vol.14 (2), p.165-173

2014

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The spatio-temporal distribution of lightning over Israel and the neighboring area and its relation to regional synoptic systems

Natural hazards and earth system sciences, 2011-08, Vol.11 (8), p.2125-2135

2011

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A Comparison Study of Middle Bronze Age II Daggers and Their Rivets as a Tool for a Better Understanding of Their Production

Archaeometry, 2018-06, Vol.60 (3), p.535-553

2018

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Number development and developmental dyscalculia

Developmental medicine and child neurology, 2007-11, Vol.49 (11), p.868-873

2007

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Digital Systems in Public Policy and Urban Planning: Lobbying, Examples, and Recommendations for Further Application

Vestnik Rossijskogo universiteta družby narodov. Seriâ Politologiâ (Online), 2023-09, Vol.25 (3), p.647-662

2023

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Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome

Prenatal diagnosis, 2006-09, Vol.26 (9), p.782-784

2006

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Parenting Style Impacts on Quality of Life in Children with Cerebral Palsy

The Journal of pediatrics, 2007-07, Vol.151 (1), p.56-60.e1

2007

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Characteristics of genetic diseases in consanguineous populations in the genomic era: Lessons from Arab communities in North Israel

Expanding the genotypic spectrum of Perrault syndrome

Desert flash floods form hyperpycnal flows in the coral-rich Gulf of Aqaba, Red Sea

Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects

Erratum to “A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery” [Int. J. Obstetric Anesth. 49 (2022) 103229]

DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation

Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small‐platelet thrombocytopenia

Obstetric quality of recovery scoring tool: assessment of validity, reliability and feasibility in an Israeli cesarean delivery population

A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery

THU0222 The Diagnosis of Familial Mediterranean Fever Following The Initial Presentation of Monoarthritis

Distinguishability between ancient and modern leaded tin bronzes by the composition of their lead inclusions

Developmental Dyscalculia

Severe infantile male encephalopathy is a result of early post-zygotic WDR45 somatic mutation

Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10

Developmental dyscalculia: a prospective six-year follow-up

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans

Lightning flash multiplicity in eastern Mediterranean thunderstorms

The spatio-temporal distribution of lightning over Israel and the neighboring area and its relation to regional synoptic systems

A Comparison Study of Middle Bronze Age II Daggers and Their Rivets as a Tool for a Better Understanding of Their Production

Number development and developmental dyscalculia

Digital Systems in Public Policy and Urban Planning: Lobbying, Examples, and Recommendations for Further Application

Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome

Parenting Style Impacts on Quality of Life in Children with Cerebral Palsy

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