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Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders
Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders
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Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders

Manelis-Baram, Liora ; Meiri, Gal ; Ilan, Michal ; Faroy, Michal ; Michaelovski, Analya ; Flusser, Hagit ; Menashe, Idan ; Dinstein, Ilan

Journal of autism and developmental disorders, 2022-02, Vol.52 (2), p.923-937 [Periódico revisado por pares]

New York: Springer US

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Comorbidity and health services' usage in children with autism spectrum disorder: a nested case-control study
Comorbidity and health services' usage in children with autism spectrum disorder: a nested case-control study
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Comorbidity and health services' usage in children with autism spectrum disorder: a nested case-control study

Dizitzer, Yotam ; Meiri, Gal ; Flusser, Hagit ; Michaelovski, Analya ; Dinstein, Ilan ; Menashe, Idan

Epidemiology and psychiatric sciences, 2020-01, Vol.29, p.e95-e95, Article e95 [Periódico revisado por pares]

England: Cambridge University Press

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3
Hypofractionated adjuvant radiation therapy of soft-tissue sarcoma achieves excellent results in elderly patients
Hypofractionated adjuvant radiation therapy of soft-tissue sarcoma achieves excellent results in elderly patients
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Hypofractionated adjuvant radiation therapy of soft-tissue sarcoma achieves excellent results in elderly patients

Soyfer, V ; Corn, B W ; Kollender, Y ; Issakov, J ; Dadia, S ; Flusser, G ; Bickels, J ; Meller, I ; Merimsky, O

British journal of radiology, 2013-08, Vol.86 (1028), p.20130258-20130258 [Periódico revisado por pares]

England: The British Institute of Radiology

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4
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome
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SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome

Wormser, Ohad ; Gradstein, Libe ; Yogev, Yuval ; Perez, Yonatan ; Kadir, Rotem ; Goliand, Inna ; Sadka, Yair ; El Riati, Saad ; Flusser, Hagit ; Nachmias, Dikla ; Birk, Ruth ; Iraqi, Muhamad ; Kadar, Einat ; Gat, Roni ; Drabkin, Max ; Halperin, Daniel ; Horev, Amir ; Sivan, Sara ; Abdu, Uri ; Elia, Natalie ; Birk, Ohad S

European journal of human genetics : EJHG, 2019-06, Vol.27 (6), p.928-940 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Lactococcus garvieae Endocarditis on a Prosthetic Biological Aortic Valve
Lactococcus garvieae Endocarditis on a Prosthetic Biological Aortic Valve
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Lactococcus garvieae Endocarditis on a Prosthetic Biological Aortic Valve

Tsur, A. ; Slutzki, T. ; Flusser, D.

Zoonoses and public health, 2015-09, Vol.62 (6), p.435-437 [Periódico revisado por pares]

Germany: Blackwell Verlag

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6
Quantifying the social symptoms of autism using motion capture
Quantifying the social symptoms of autism using motion capture
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Quantifying the social symptoms of autism using motion capture

Budman, Ian ; Meiri, Gal ; Ilan, Michal ; Faroy, Michal ; Langer, Allison ; Reboh, Doron ; Michaelovski, Analya ; Flusser, Hagit ; Menashe, Idan ; Donchin, Opher ; Dinstein, Ilan

Scientific reports, 2019-05, Vol.9 (1), p.7712-7712, Article 7712 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish
Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish
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Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish

Perez, Yonatan ; Bar-Yaacov, Reut ; Kadir, Rotem ; Wormser, Ohad ; Shelef, Ilan ; Birk, Ohad S ; Flusser, Hagit ; Birnbaum, Ramon Y

Brain (London, England : 1878), 2019-03, Vol.142 (3), p.574-585 [Periódico revisado por pares]

England: Oxford University Press

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8
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN
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UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN

Perez, Yonatan ; Kadir, Rotem ; Volodarsky, Michael ; Noyman, Iris ; Flusser, Hagit ; Shorer, Zamir ; Gradstein, Libe ; Birnbaum, Ramon Y ; Birk, Ohad S

Journal of medical genetics, 2016-06, Vol.53 (6), p.397-402 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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9
A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta
A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta
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A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta

Volodarsky, Michael ; Markus, Barak ; Cohen, Idan ; Staretz-Chacham, Orna ; Flusser, Hagit ; Landau, Daniella ; Shelef, Ilan ; Langer, Yshaia ; Birk, Ohad S.

Human mutation, 2013-04, Vol.34 (4), p.582-586 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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10
Utilizing MR enterography for detection of sacroiliitis in patients with inflammatory bowel disease
Utilizing MR enterography for detection of sacroiliitis in patients with inflammatory bowel disease
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Utilizing MR enterography for detection of sacroiliitis in patients with inflammatory bowel disease

Gotler, Jakob ; Amitai, Michal M. ; Lidar, Merav ; Aharoni, Dvora ; Flusser, Gideon ; Eshed, Iris

Journal of magnetic resonance imaging, 2015-07, Vol.42 (1), p.121-127 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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