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Fetal alcohol spectrum disorder among pre-adopted and foster children

BMC pediatrics, 2020-06, Vol.20 (1), p.275-6, Article 275

2020

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Attitudes Toward Attention-Deficit Hyperactivity Disorder (ADHD) Treatment: Parents' and Children's Perspectives

Journal of child neurology, 2008-09, Vol.23 (9), p.1036-1042

2008

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Microvascular Patterning Is Controlled by Fine-Tuning the Akt Signal

Proceedings of the National Academy of Sciences - PNAS, 2005-01, Vol.102 (1), p.128-133

2005

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Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Neuromuscular disorders : NMD, 2017-02, Vol.27 (2), p.136-140

2017

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Young Adults and Parents’ Coping With Duchenne/Becker Muscular Dystrophy: A Focus Group Study

Emerging adulthood (Thousand Oaks, CA), 2024-08, Vol.12 (4), p.481-493

2024

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Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1)

Muscle & nerve, 2016-04, Vol.53 (4), p.564-569

2016

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A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness

American journal of medical genetics. Part A, 2018-01, Vol.176 (1), p.92-98

2018

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Neurological and neurodevelopmental symptoms in children with familial Mediterranean fever and their siblings

European journal of pediatrics, 2022-03, Vol.181 (3), p.973-978

2022

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Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome

Journal of medical genetics, 2017-08, Vol.54 (8), p.558-566

2017

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Vessel maturation schedule determines vulnerability to neuronal injuries of prematurity

The Journal of clinical investigation, 2015-03, Vol.125 (3), p.1319-1328

2015

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A homozygous deleterious mutation in CDK10 is associated with agenesis of corpus callosum, retinopathy and deafness

American journal of medical genetics. Part A, 2017-11, Vol.176 (1), p.92-98

2017

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A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness

American journal of medical genetics. Part A, 2017-11

2017

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Fetal alcohol spectrum disorder in Israel: increased prevalence in an at-risk population

The Israel Medical Association journal, 2011-12, Vol.13 (12), p.725-729

2011

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Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing

Molecular genetics and metabolism, 2011-12, Vol.104 (4), p.517-520

2011

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Periventricular leukomalacia in premature infants: from pathogenesis to treatment

הרפואה, 2008-02, Vol.147 (2), p.159

2008

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Early peripheral nervous system manifestations of infantile Krabbe disease

Pediatric neurology, 2003-02, Vol.28 (2), p.115-118

2003

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Evidence for increased breakthrough rates of SARS-CoV-2 variants of concern in BNT162b2-mRNA-vaccinated individuals

Nature medicine, 2021-08, Vol.27 (8), p.1379-1384

2021

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Identification of tissue-specific cell death using methylation patterns of circulating DNA

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (13), p.E1826-E1834

2016

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Monitoring the ovaries after autotransplantation of cryopreserved ovarian tissue: endocrine studies, in vitro fertilization cycles, and live birth

Fertility and sterility, 2007-02, Vol.87 (2), p.418.e7-418.e15

2007

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Pregnancy after Transplantation of Cryopreserved Ovarian Tissue in a Patient with Ovarian Failure after Chemotherapy

The New England journal of medicine, 2005-07, Vol.353 (3), p.318-321

2005

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The differential regulation of placenta trophoblast bisphosphoglycerate mutase in fetal growth restriction: preclinical study in mice and observational histological study of human placenta

eLife, 2024-02, Vol.13

2024

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Hallmarks of transcriptional intratumour heterogeneity across a thousand tumours

Nature (London), 2023-06, Vol.618 (7965), p.598-606

2023

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The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variants

Cancer, 2024-01, Vol.130 (2), p.256-266

2024

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The connection between North Atlantic storm track regimes and eastern Mediterranean cyclonic activity

Weather and climate dynamics, 2024-09, Vol.5 (3), p.1103-1116

2024

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Fetal alcohol spectrum disorder among pre-adopted and foster children

Attitudes Toward Attention-Deficit Hyperactivity Disorder (ADHD) Treatment: Parents' and Children's Perspectives

Microvascular Patterning Is Controlled by Fine-Tuning the Akt Signal

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Young Adults and Parents’ Coping With Duchenne/Becker Muscular Dystrophy: A Focus Group Study

Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1)

A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness

Neurological and neurodevelopmental symptoms in children with familial Mediterranean fever and their siblings

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome

Ataluren treatment of patients with nonsense mutation dystrophinopathy

Vessel maturation schedule determines vulnerability to neuronal injuries of prematurity

A homozygous deleterious mutation in CDK10 is associated with agenesis of corpus callosum, retinopathy and deafness

A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness

Fetal alcohol spectrum disorder in Israel: increased prevalence in an at-risk population

Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing

Periventricular leukomalacia in premature infants: from pathogenesis to treatment

Early peripheral nervous system manifestations of infantile Krabbe disease

Evidence for increased breakthrough rates of SARS-CoV-2 variants of concern in BNT162b2-mRNA-vaccinated individuals

Identification of tissue-specific cell death using methylation patterns of circulating DNA

Monitoring the ovaries after autotransplantation of cryopreserved ovarian tissue: endocrine studies, in vitro fertilization cycles, and live birth

Pregnancy after Transplantation of Cryopreserved Ovarian Tissue in a Patient with Ovarian Failure after Chemotherapy

The differential regulation of placenta trophoblast bisphosphoglycerate mutase in fetal growth restriction: preclinical study in mice and observational histological study of human placenta

Hallmarks of transcriptional intratumour heterogeneity across a thousand tumours

The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variants

The connection between North Atlantic storm track regimes and eastern Mediterranean cyclonic activity

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