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Items: 34

1.

False Interpretation of Scientific Data Leads to Biased Conclusions About the Association Between Cesarean Deliveries Under General Anesthesia and Risk of Autism Spectrum Disorder.

Menashe I, Dinstein I, Flusser H, Michaelovski A, Bashiri A, Meiri G.

J Autism Dev Disord. 2020 Feb 19. doi: 10.1007/s10803-020-04415-5. [Epub ahead of print] No abstract available.

PMID:
32076958
2.

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

Dizitzer Y, Meiri G, Flusser H, Michaelovski A, Dinstein I, Menashe I.

Epidemiol Psychiatr Sci. 2020 Jan 28;29:e95. doi: 10.1017/S2045796020000050.

PMID:
31987063
3.

Reduced sleep pressure in young children with autism.

Arazi A, Meiri G, Danan D, Michaelovski A, Flusser H, Menashe I, Tarasiuk A, Dinstein I.

Sleep. 2019 Dec 18. pii: zsz309. doi: 10.1093/sleep/zsz309. [Epub ahead of print]

PMID:
31848619
4.

Children with autism observe social interactions in an idiosyncratic manner.

Avni I, Meiri G, Bar-Sinai A, Reboh D, Manelis L, Flusser H, Michaelovski A, Menashe I, Dinstein I.

Autism Res. 2019 Oct 26. doi: 10.1002/aur.2234. [Epub ahead of print]

PMID:
31654504
5.

Language regression is associated with faster early motor development in children with autism spectrum disorder.

Manelis L, Meiri G, Ilan M, Flusser H, Michaelovski A, Faroy M, Kerub O, Dinstein I, Menashe I.

Autism Res. 2020 Jan;13(1):145-156. doi: 10.1002/aur.2197. Epub 2019 Aug 30.

PMID:
31468744
6.

Quantifying the social symptoms of autism using motion capture.

Budman I, Meiri G, Ilan M, Faroy M, Langer A, Reboh D, Michaelovski A, Flusser H, Menashe I, Donchin O, Dinstein I.

Sci Rep. 2019 May 22;9(1):7712. doi: 10.1038/s41598-019-44180-9.

7.

Exposure to General Anesthesia May Contribute to the Association between Cesarean Delivery and Autism Spectrum Disorder.

Huberman Samuel M, Meiri G, Dinstein I, Flusser H, Michaelovski A, Bashiri A, Menashe I.

J Autism Dev Disord. 2019 Aug;49(8):3127-3135. doi: 10.1007/s10803-019-04034-9.

PMID:
31053992
8.

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

Wormser O, Gradstein L, Yogev Y, Perez Y, Kadir R, Goliand I, Sadka Y, El Riati S, Flusser H, Nachmias D, Birk R, Iraqi M, Kadar E, Gat R, Drabkin M, Halperin D, Horev A, Sivan S, Abdu U, Elia N, Birk OS.

Eur J Hum Genet. 2019 Jun;27(6):928-940. doi: 10.1038/s41431-019-0347-z. Epub 2019 Feb 5.

PMID:
30723319
9.

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

Perez Y, Bar-Yaacov R, Kadir R, Wormser O, Shelef I, Birk OS, Flusser H, Birnbaum RY.

Brain. 2019 Mar 1;142(3):574-585. doi: 10.1093/brain/awz004.

10.

SEC31A mutation affects ER homeostasis, causing a neurological syndrome.

Halperin D, Kadir R, Perez Y, Drabkin M, Yogev Y, Wormser O, Berman EM, Eremenko E, Rotblat B, Shorer Z, Gradstein L, Shelef I, Birk R, Abdu U, Flusser H, Birk OS.

J Med Genet. 2019 Mar;56(3):139-148. doi: 10.1136/jmedgenet-2018-105503. Epub 2018 Nov 21.

PMID:
30464055
11.

Malignant Peritoneal Mesothelioma in an Infant With Familial ATM Mutations.

Mijalovsky A, Halperin D, Perez Y, Zafarov B, Shaco-Levy R, Kapelushnik J, Flusser H, Birk OS.

J Pediatr Hematol Oncol. 2018 Nov;40(8):e511-e515. doi: 10.1097/MPH.0000000000001294.

PMID:
30124550
12.

Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 disease.

Flusser H, Halperin D, Kadir R, Shorer Z, Shelef I, Birk OS.

Clin Genet. 2018 Nov;94(5):473-479. doi: 10.1111/cge.13419. Epub 2018 Aug 9.

PMID:
30039846
13.

Sleep disturbances are associated with specific sensory sensitivities in children with autism.

Tzischinsky O, Meiri G, Manelis L, Bar-Sinai A, Flusser H, Michaelovski A, Zivan O, Ilan M, Faroy M, Menashe I, Dinstein I.

Mol Autism. 2018 Mar 27;9:22. doi: 10.1186/s13229-018-0206-8. eCollection 2018.

14.

PAX7 mutation in a syndrome of failure to thrive, hypotonia, and global neurodevelopmental delay.

Proskorovski-Ohayon R, Kadir R, Michalowski A, Flusser H, Perez Y, Hershkovitz E, Sivan S, Birk OS.

Hum Mutat. 2017 Dec;38(12):1671-1683. doi: 10.1002/humu.23310. Epub 2017 Sep 22.

PMID:
28779497
15.

Brief Report: The Negev Hospital-University-Based (HUB) Autism Database.

Meiri G, Dinstein I, Michaelowski A, Flusser H, Ilan M, Faroy M, Bar-Sinai A, Manelis L, Stolowicz D, Yosef LL, Davidovitch N, Golan H, Arbelle S, Menashe I.

J Autism Dev Disord. 2017 Sep;47(9):2918-2926. doi: 10.1007/s10803-017-3207-0.

PMID:
28631035
16.

Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.

Yogev Y, Perez Y, Noyman I, Madegem AA, Flusser H, Shorer Z, Cohen E, Kachko L, Michaelovsky A, Birk R, Koifman A, Drabkin M, Wormser O, Halperin D, Kadir R, Birk OS.

Eur J Hum Genet. 2017 Aug;25(8):966-972. doi: 10.1038/ejhg.2017.85. Epub 2017 May 10.

17.

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 Y, Kadir R, Volodarsky M, Noyman I, Flusser H, Shorer Z, Gradstein L, Birnbaum RY, Birk OS.

J Med Genet. 2016 Jun;53(6):397-402. doi: 10.1136/jmedgenet-2015-103352. Epub 2015 Nov 6.

PMID:
26545877
18.

A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A.

Fine D, Flusser H, Markus B, Shorer Z, Gradstein L, Khateeb S, Langer Y, Narkis G, Birk R, Galil A, Shelef I, Birk OS.

Eur J Hum Genet. 2015 Dec;23(12):1729-34. doi: 10.1038/ejhg.2014.241. Epub 2014 Nov 12.

19.

VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2).

Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS.

J Med Genet. 2014 May;51(5):303-8. doi: 10.1136/jmedgenet-2013-101823. Epub 2014 Feb 27.

PMID:
24577744
20.

Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation.

Perez Y, Gradstein L, Flusser H, Markus B, Cohen I, Langer Y, Marcus M, Lifshitz T, Kadir R, Birk OS.

Eur J Hum Genet. 2014 May;22(5):703-6. doi: 10.1038/ejhg.2013.212. Epub 2013 Sep 18.

21.

A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta.

Volodarsky M, Markus B, Cohen I, Staretz-Chacham O, Flusser H, Landau D, Shelef I, Langer Y, Birk OS.

Hum Mutat. 2013 Apr;34(4):582-6. doi: 10.1002/humu.22274.

PMID:
23316006
22.

The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matter.

Zolotushko J, Flusser H, Markus B, Shelef I, Langer Y, Heverin M, Björkhem I, Sivan S, Birk OS.

Eur J Hum Genet. 2011 Sep;19(9):942-6. doi: 10.1038/ejhg.2011.74. Epub 2011 May 11.

23.

Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.

Feinstein M, Markus B, Noyman I, Shalev H, Flusser H, Shelef I, Liani-Leibson K, Shorer Z, Cohen I, Khateeb S, Sivan S, Birk OS.

Am J Hum Genet. 2010 Dec 10;87(6):820-8. doi: 10.1016/j.ajhg.2010.10.016. Epub 2010 Nov 18.

24.

Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy.

Agamy O, Ben Zeev B, Lev D, Marcus B, Fine D, Su D, Narkis G, Ofir R, Hoffmann C, Leshinsky-Silver E, Flusser H, Sivan S, Söll D, Lerman-Sagie T, Birk OS.

Am J Hum Genet. 2010 Oct 8;87(4):538-44. doi: 10.1016/j.ajhg.2010.09.007.

25.

Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ.

Barel O, Shorer Z, Flusser H, Ofir R, Narkis G, Finer G, Shalev H, Nasasra A, Saada A, Birk OS.

Am J Hum Genet. 2008 May;82(5):1211-6. doi: 10.1016/j.ajhg.2008.03.020. Epub 2008 Apr 24.

26.

Pediatricians' communication styles as correlates of global trust among Jewish and Bedouin parents of disabled children.

Kushnir T, Bachner YG, Carmel S, Flusser H, Galil A.

J Dev Behav Pediatr. 2008 Feb;29(1):18-25. doi: 10.1097/DBP.0b013e3181469016.

PMID:
18300724
27.

PLA2G6 mutation underlies infantile neuroaxonal dystrophy.

Khateeb S, Flusser H, Ofir R, Shelef I, Narkis G, Vardi G, Shorer Z, Levy R, Galil A, Elbedour K, Birk OS.

Am J Hum Genet. 2006 Nov;79(5):942-8. Epub 2006 Sep 19.

28.

Physician-parent communication as predictor of parent satisfaction with child development services.

Galil A, Bachner YG, Merrick J, Flusser H, Lubetzky H, Heiman N, Carmel S.

Res Dev Disabil. 2006 May-Jun;27(3):233-42. Epub 2005 Jul 5.

PMID:
15998579
29.

Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation.

Flusser H, Korman SH, Sato K, Matsubara Y, Galil A, Kure S.

Neurology. 2005 Apr 26;64(8):1426-30.

PMID:
15851735
30.

COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED).

Harel T, Rabinowitz R, Hendler N, Galil A, Flusser H, Chemke J, Gradstein L, Lifshitz T, Ofir R, Elbedour K, Birk OS.

Am J Med Genet A. 2005 Jan 1;132A(1):33-5.

PMID:
15558753
31.

Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III.

Raas-Rothschild A, Bargal R, Goldman O, Ben-Asher E, Groener JE, Toutain A, Stemmer E, Ben-Neriah Z, Flusser H, Beemer FA, Penttinen M, Olender T, Rein AJ, Bach G, Zeigler M.

J Med Genet. 2004 Apr;41(4):e52. No abstract available.

32.

Neurodevelopmental outcome and respiratory morbidity for extracorporeal membrane oxygenation survivors at 1 year of age.

Flusser H, Dodge NN, Engle WE, Garg BP, West KW.

J Perinatol. 1993 Jul-Aug;13(4):266-71.

PMID:
7692022
33.

Basilar migraine manifesting as transient global amnesia in a 9-year-old child.

Amit R, Shapira Y, Flusser H, Aker M.

Headache. 1986 Jan;26(1):17-8. No abstract available.

PMID:
3781819
34.

[Glossodynia: sensation of burn in the oral cavity].

ACH MS, ANDELOVA E, CHVOJKOVA V, FLUSSER H.

Revue Stomatol. 1954 Feb-Mar;55(2-3):136-41. Undetermined Language. No abstract available.

PMID:
15444571

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