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Items: 1 to 50 of 401

1.

What nonpharmacological therapeutic interventions are provided to adolescents admitted to general mental health inpatient units? A descriptive review.

Hayes C, Palmer V, Hamilton B, Simons C, Hopwood M.

Int J Ment Health Nurs. 2019 Feb 12. doi: 10.1111/inm.12575. [Epub ahead of print] Review.

PMID:
30756470
2.

Cerebral hypomyelination associated with biallelic variants of FIG4.

Lenk GM, Berry IR, Stutterd CA, Blyth M, Green L, Vadlamani G, Warren D, Craven I, Fanjul-Fernandez M, Rodriguez-Casero V, Lockhart PJ, Vanderver A, Simons C, Gibb S, Sadedin S; Broad Center for Mendelian Genomics, White SM, Christodoulou J, Skibina O, Ruddle J, Tan TY, Leventer RJ, Livingston JH, Meisler MH.

Hum Mutat. 2019 Feb 10. doi: 10.1002/humu.23720. [Epub ahead of print]

PMID:
30740813
3.

Synthesis and anti-HSV activity of tricyclic penciclovir and hydroxybutylguanine derivatives.

Mohammed AF, Andrei G, Hayallah AM, Abdel-Moty SG, Snoeck R, Simons C.

Bioorg Med Chem. 2019 Feb 2. pii: S0968-0896(18)32087-X. doi: 10.1016/j.bmc.2019.02.005. [Epub ahead of print]

PMID:
30738653
4.

Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy.

van der Knaap MS, Bugiani M, Mendes MI, Riley LG, Smith DEC, Rudinger-Thirion J, Frugier M, Breur M, Crawford J, van Gaalen J, Schouten M, Willems M, Waisfisz Q, Mau-Them FT, Rodenburg RJ, Taft RJ, Keren B, Christodoulou J, Depienne C, Simons C, Salomons GS, Mochel F.

Neurology. 2019 Feb 8. pii: 10.1212/WNL.0000000000007098. doi: 10.1212/WNL.0000000000007098. [Epub ahead of print]

PMID:
30737337
5.
6.

Hybrid LSTM and Encoder-Decoder Architecture for Detection of Image Forgeries.

Bappy JH, Simons C, Nataraj L, Manjunath BS, Roy-Chowdhury AK.

IEEE Trans Image Process. 2019 Jan 25. doi: 10.1109/TIP.2019.2895466. [Epub ahead of print]

PMID:
30703026
7.

Lysosomal dysfunction in TMEM106B hypomyelinating leukodystrophy.

Ito Y, Hartley T, Baird S, Venkateswaran S, Simons C, Wolf NI, Boycott KM, Dyment DA, Kernohan KD.

Neurol Genet. 2018 Nov 13;4(6):e288. doi: 10.1212/NXG.0000000000000288. eCollection 2018 Dec. No abstract available.

8.

Leukoencephalopathy due to variants in GFPT1-associated congenital myasthenic syndrome.

Helman G, Sharma S, Crawford J, Patra B, Jain P, Bent SJ, Urtizberea JA, Saran RK, Taft RJ, van der Knaap MS, Simons C.

Neurology. 2019 Feb 5;92(6):e587-e593. doi: 10.1212/WNL.0000000000006886. Epub 2019 Jan 11.

PMID:
30635494
9.

Patterns of obsessive-compulsive symptoms and social functioning in schizophrenia; a replication study.

Swets M, van Dijk FA, Schirmbeck F, Peen J, de Haan L, Alizadeh BZ, van Amelsvoort T, Bartels-Velthuis AA, van Beveren NJ, Bruggeman R, Cahn W, Delespaul P, Luykx JJ, Myin-Germeys I, Kahn RS, Simons CJP, van Haren NE, van Os J, van Winkel R.

Psychiatry Res. 2019 Jan;271:421-427. doi: 10.1016/j.psychres.2018.11.071. Epub 2018 Dec 3.

PMID:
30537664
10.

Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches.

Backhouse B, Hanna C, Robevska G, van den Bergen J, Pelosi E, Simons C, Koopman P, Juniarto AZ, Grover S, Faradz S, Sinclair A, Ayers K, Tan TY.

Sex Dev. 2018 Dec 1. doi: 10.1159/000494896. [Epub ahead of print]

PMID:
30504698
11.

Correction: Cognitive Performance and Long-Term Social Functioning in Psychotic Disorder: A Three-Year Follow-Up Study.

Simons CJP, Bartels-Velthuis AA, Pijnenborg GHM; Genetic Risk and Outcome of Psychosis (GROUP) Investigators.

PLoS One. 2018 Nov 26;13(11):e0208347. doi: 10.1371/journal.pone.0208347. eCollection 2018.

12.

Sirtuin 1 genetic variation, energy balance and colorectal cancer risk by sex and subsite in the Netherlands Cohort Study.

Simons CCJM, Schouten LJ, Godschalk RW, van Schooten FJ, van den Brandt PA, Weijenberg MP.

Sci Rep. 2018 Nov 8;8(1):16540. doi: 10.1038/s41598-018-34728-6.

13.

Effect of self-monitoring through experience sampling on emotion differentiation in depression.

Widdershoven RLA, Wichers M, Kuppens P, Hartmann JA, Menne-Lothmann C, Simons CJP, Bastiaansen JA.

J Affect Disord. 2019 Feb 1;244:71-77. doi: 10.1016/j.jad.2018.10.092. Epub 2018 Oct 6.

PMID:
30321767
14.

Corrigendum to "Long-term course of negative symptom subdomains and relationship with outcome in patients with a psychotic disorder" [Schizophr. Res. 193 (2018) 173-181].

Stiekema APM, Islam MA, Liemburg EJ, Castelein S, van den Heuvel ER, van Weeghel J, Aleman A, Bruggeman R, van der Meer L; GROUP investigators, Alizadeh BZ, Bartels-Velthuis AA, van Beveren NJ, Bruggeman R, Cahn W, de Haan L, Delespaul P, Meijer CJ, Myin-Germeys I, Kahn RS, Schirmbeck F, Simons CJP, van Haren NEM, van Os J, van Winkel R.

Schizophr Res. 2018 Oct 9. pii: S0920-9964(18)30605-4. doi: 10.1016/j.schres.2018.10.003. [Epub ahead of print] No abstract available.

PMID:
30314649
15.

Associations of adult-attained height and early life energy restriction with postmenopausal breast cancer risk according to estrogen and progesterone receptor status.

Elands RJJ, Offermans NSM, Simons CCJM, Schouten LJ, Verhage BA, van den Brandt PA, Weijenberg MP.

Int J Cancer. 2019 Apr 15;144(8):1844-1857. doi: 10.1002/ijc.31890. Epub 2018 Nov 9.

PMID:
30252931
16.

Reasoning bias, working memory performance and a transdiagnostic phenotype of affective disturbances and psychotic experiences in the general population.

Reininghaus U, Rauschenberg C, Ten Have M, de Graaf R, van Dorsselaer S, Simons CJP, Gunther N, Pries LK, Guloksuz S, Radhakrishnan R, Bak M, van Os J.

Psychol Med. 2018 Aug 30:1-11. doi: 10.1017/S0033291718002209. [Epub ahead of print]

PMID:
30160228
17.

Alcohol drinking, ADH1B and ADH1C genotypes and the risk of postmenopausal breast cancer by hormone receptor status: the Netherlands Cohort Study on diet and cancer.

Hahn M, Simons CCJM, Weijenberg MP, van den Brandt PA.

Carcinogenesis. 2018 Dec 13;39(11):1342-1351. doi: 10.1093/carcin/bgy101.

PMID:
30052783
18.

Accessing Care Through the Veterans Choice Program: The Veteran Experience.

Sayre GG, Neely EL, Simons CE, Sulc CA, Au DH, Michael Ho P.

J Gen Intern Med. 2018 Oct;33(10):1714-1720. doi: 10.1007/s11606-018-4574-8. Epub 2018 Jul 23.

PMID:
30039494
19.

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy.

McMillan HJ, Telegrafi A, Singleton A, Cho MT, Lelli D, Lynn FC, Griffin J, Asamoah A, Rinne T, Erasmus CE, Koolen DA, Haaxma CA, Keren B, Doummar D, Mignot C, Thompson I, Velsher L, Dehghani M, Vahidi Mehrjardi MY, Maroofian R, Tchan M, Simons C, Christodoulou J, Martín-Hernández E, Guillen Sacoto MJ, Henderson LB, McLaughlin H, Molday LL, Molday RS, Yoon G.

Orphanet J Rare Dis. 2018 May 31;13(1):86. doi: 10.1186/s13023-018-0825-3.

20.

Different Olfactory Percepts Evoked by Orthonasal and Retronasal Odorant Delivery.

Hannum M, Stegman MA, Fryer JA, Simons CT.

Chem Senses. 2018 Aug 24;43(7):515-521. doi: 10.1093/chemse/bjy043.

PMID:
29982522
21.

Comparative tactile sensitivity of the fingertip and apical tongue using complex and pure tactile tasks.

Miles BL, Van Simaeys K, Whitecotton M, Simons CT.

Physiol Behav. 2018 Oct 1;194:515-521. doi: 10.1016/j.physbeh.2018.07.002. Epub 2018 Jul 5.

PMID:
29981764
22.

Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and Arthrogryposis.

Conant A, Curiel J, Pizzino A, Sabetrasekh P, Murphy J, Bloom M, Evans SH, Helman G, Taft RJ, Simons C, Whitehead MT, Moore SA, Vanderver A.

J Child Neurol. 2018 Sep;33(10):642-650. doi: 10.1177/0883073818776157. Epub 2018 Jun 8.

PMID:
29882456
23.

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms.

Forbes TA, Howden SE, Lawlor K, Phipson B, Maksimovic J, Hale L, Wilson S, Quinlan C, Ho G, Holman K, Bennetts B, Crawford J, Trnka P, Oshlack A, Patel C, Mallett A, Simons C, Little MH.

Am J Hum Genet. 2018 May 3;102(5):816-831. doi: 10.1016/j.ajhg.2018.03.014. Epub 2018 Apr 26.

24.

Mutations in SZT2 result in early-onset epileptic encephalopathy and leukoencephalopathy.

Pizzino A, Whitehead M, Sabet Rasekh P, Murphy J, Helman G, Bloom M, Evans SH, Murnick JG, Conry J, Taft RJ, Simons C, Vanderver A, Adang LA.

Am J Med Genet A. 2018 Jun;176(6):1443-1448. doi: 10.1002/ajmg.a.38717. Epub 2018 Apr 25.

PMID:
29696782
25.

Severe Leukoencephalopathy with Clinical Recovery Caused by Recessive BOLA3 Mutations.

Stutterd CA, Lake NJ, Peters H, Lockhart PJ, Taft RJ, van der Knaap MS, Vanderver A, Thorburn DR, Simons C, Leventer RJ.

JIMD Rep. 2019;43:63-70. doi: 10.1007/8904_2018_100. Epub 2018 Apr 14.

26.

Research protocol: The initiation, design and establishment of the Global Angelman Syndrome Registry.

Tones M, Cross M, Simons C, Napier KR, Hunter A, Bellgard MI, Heussler H.

J Intellect Disabil Res. 2018 May;62(5):431-443. doi: 10.1111/jir.12482.

PMID:
29633452
27.

Expression Pattern of the Aspartyl-tRNA Synthetase DARS in the Human Brain.

Fröhlich D, Suchowerska AK, Voss C, He R, Wolvetang E, von Jonquieres G, Simons C, Fath T, Housley GD, Klugmann M.

Front Mol Neurosci. 2018 Mar 20;11:81. doi: 10.3389/fnmol.2018.00081. eCollection 2018.

28.

Functional Properties of a High Protein Beverage Stabilized with Oat-β-Glucan.

Vasquez-Orejarena E, Simons CT, Litchfield JH, Alvarez VB.

J Food Sci. 2018 May;83(5):1360-1365. doi: 10.1111/1750-3841.14119. Epub 2018 Mar 30.

PMID:
29603228
29.

Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy.

Mendes MI, Gutierrez Salazar M, Guerrero K, Thiffault I, Salomons GS, Gauquelin L, Tran LT, Forget D, Gauthier MS, Waisfisz Q, Smith DEC, Simons C, van der Knaap MS, Marquardt I, Lemes A, Mierzewska H, Weschke B, Koehler W, Coulombe B, Wolf NI, Bernard G.

Am J Hum Genet. 2018 Apr 5;102(4):676-684. doi: 10.1016/j.ajhg.2018.02.011. Epub 2018 Mar 22.

30.

Reply: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot.

Simons C, Dyment D, van der Knaap MS, Wolf NI.

Brain. 2018 May 1;141(5):e37. doi: 10.1093/brain/awy030. No abstract available.

PMID:
29444246
31.

Olfactory Adaptation is Dependent on Route of Delivery.

Pierce AM, Simons CT.

Chem Senses. 2018 Feb 26;43(3):197-203. doi: 10.1093/chemse/bjy007.

PMID:
29401258
32.

Alcohol intake, ADH1B and ADH1C genotypes, and the risk of colorectal cancer by sex and subsite in the Netherlands Cohort Study.

Offermans NSM, Ketcham SM, van den Brandt PA, Weijenberg MP, Simons CCJM.

Carcinogenesis. 2018 Mar 8;39(3):375-388. doi: 10.1093/carcin/bgy011.

PMID:
29390059
33.

Consumer acceptability of gluten-free cookies containing raw cooked and germinated pinto bean flours.

Simons CW, Hall C 3rd.

Food Sci Nutr. 2017 Nov 20;6(1):77-84. doi: 10.1002/fsn3.531. eCollection 2018 Jan.

34.

Subjective quality of life in psychosis: Evidence for an association with real world functioning?

Leendertse P, Myin-Germeys I, Lataster T, Simons CJP, Oorschot M, Lardinois M, Schneider M, van Os J, Reininghaus U; For Genetic Risk and Outcome of Psychosis (GROUP) investigators.

Psychiatry Res. 2018 Mar;261:116-123. doi: 10.1016/j.psychres.2017.11.074. Epub 2017 Dec 6.

PMID:
29291477
35.

Economic evaluation of an experience sampling method intervention in depression compared with treatment as usual using data from a randomized controlled trial.

Simons CJP, Drukker M, Evers S, van Mastrigt GAPG, Höhn P, Kramer I, Peeters F, Delespaul P, Menne-Lothmann C, Hartmann JA, van Os J, Wichers M.

BMC Psychiatry. 2017 Dec 29;17(1):415. doi: 10.1186/s12888-017-1577-7.

36.

Lifestyle, Diet, and Colorectal Cancer Risk According to (Epi)genetic Instability: Current Evidence and Future Directions of Molecular Pathological Epidemiology.

Hughes LAE, Simons CCJM, van den Brandt PA, van Engeland M, Weijenberg MP.

Curr Colorectal Cancer Rep. 2017;13(6):455-469. doi: 10.1007/s11888-017-0395-0. Epub 2017 Dec 2. Review.

37.

Evaluating effectiveness in adolescent mental health inpatient units: A systematic review.

Hayes C, Simmons M, Simons C, Hopwood M.

Int J Ment Health Nurs. 2018 Apr;27(2):498-513. doi: 10.1111/inm.12418. Epub 2017 Dec 1. Review.

PMID:
29194885
38.

A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.

Simons C, Dyment D, Bent SJ, Crawford J, D'Hooghe M, Kohlschütter A, Venkateswaran S, Helman G, Poll-The BT, Makowski CC, Ito Y, Kernohan K, Hartley T, Waisfisz Q, Taft RJ; Care4Rare Consortium, van der Knaap MS, Wolf NI.

Brain. 2017 Dec 1;140(12):3105-3111. doi: 10.1093/brain/awx314.

39.

Novel Aryl Substituted Pyrazoles as Small Molecule Inhibitors of Cytochrome P450 CYP121A1: Synthesis and Antimycobacterial Evaluation.

Taban IM, Elshihawy HEAE, Torun B, Zucchini B, Williamson CJ, Altuwairigi D, Ngu AST, McLean KJ, Levy CW, Sood S, Marino LB, Munro AW, de Carvalho LPS, Simons C.

J Med Chem. 2017 Dec 28;60(24):10257-10267. doi: 10.1021/acs.jmedchem.7b01562. Epub 2017 Dec 7.

40.

Design, synthesis and evaluation against Mycobacterium tuberculosis of azole piperazine derivatives as dicyclotyrosine (cYY) mimics.

El-Wahab HAAA, Accietto M, Marino LB, McLean KJ, Levy CW, Abdel-Rahman HM, El-Gendy MA, Munro AW, Aboraia AS, Simons C.

Bioorg Med Chem. 2018 Jan 1;26(1):161-176. doi: 10.1016/j.bmc.2017.11.030. Epub 2017 Nov 21.

PMID:
29183661
41.

Constructing a Reward-Related Quality of Life Statistic in Daily Life-a Proof of Concept Study Using Positive Affect.

Verhagen SJW, Simons CJP, van Zelst C, Delespaul PAEG.

Front Psychol. 2017 Nov 2;8:1917. doi: 10.3389/fpsyg.2017.01917. eCollection 2017. Review.

42.

TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes.

Curiel J, Rodríguez Bey G, Takanohashi A, Bugiani M, Fu X, Wolf NI, Nmezi B, Schiffmann R, Bugaighis M, Pierson T, Helman G, Simons C, van der Knaap MS, Liu J, Padiath Q, Vanderver A.

Hum Mol Genet. 2017 Nov 15;26(22):4506-4518. doi: 10.1093/hmg/ddx338.

PMID:
28973395
43.

Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy.

Dorboz I, Aiello C, Simons C, Stone RT, Niceta M, Elmaleh M, Abuawad M, Doummar D, Bruselles A, Wolf NI, Travaglini L, Boespflug-Tanguy O, Tartaglia M, Vanderver A, Rodriguez D, Bertini E.

Brain. 2017 Oct 1;140(10):2550-2556. doi: 10.1093/brain/awx207.

PMID:
28969374
45.

Performance of Current Thromboembolism Risk Assessment Tools in Patients With Gastric Cancer and Validity After First Treatment.

Fuentes HE, Paz LH, Wang Y, Oramas DM, Simons CR, Tafur AJ.

Clin Appl Thromb Hemost. 2018 Jul;24(5):790-796. doi: 10.1177/1076029617726599. Epub 2017 Sep 8.

PMID:
28884610
46.

Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy.

Perrier S, Gauquelin L, Tétreault M, Tran LT, Webb N, Srour M, Mitchell JJ, Brunel-Guitton C, Majewski J, Long V, Keller S, Gambello MJ, Simons C; Care4Rare Canada Consortium, Vanderver A, Bernard G.

Clin Genet. 2018 Feb;93(2):396-400. doi: 10.1111/cge.13126. Epub 2017 Dec 21.

PMID:
28857146
47.

An experience sampling study on the ecological validity of the SWN-20: Indication that subjective well-being is associated with momentary affective states above and beyond psychosis susceptibility.

Pos K, de Wit IE, van Dijk FA, Bartels-Velthuis AA, Bruggeman R, Meijer CJ, de Haan L; for Group; Genetic Risk and Outcome of Psychosis investigators, Alizadeh BZ, Bartels-Velthuis AA, Van Beveren NJ, Bruggeman R, Cahn W, de Haan L, Delespaul P, Meijer CJ, Myin-Germeys I, Kahn RS, Schirmbeck F, Simons CJP, van Haren NE, van Os J, van Winkel R.

Psychiatry Res. 2017 Dec;258:234-238. doi: 10.1016/j.psychres.2017.08.017. Epub 2017 Aug 18.

PMID:
28851542
48.

X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1.

Miyake N, Wolf NI, Cayami FK, Crawford J, Bley A, Bulas D, Conant A, Bent SJ, Gripp KW, Hahn A, Humphray S, Kimura-Ohba S, Kingsbury Z, Lajoie BR, Lal D, Micha D, Pizzino A, Sinke RJ, Sival D, Stolte-Dijkstra I, Superti-Furga A, Ulrick N, Taft RJ, Ogata T, Ozono K, Matsumoto N, Neubauer BA, Simons C, Vanderver A.

Neurogenetics. 2017 Dec;18(4):185-194. doi: 10.1007/s10048-017-0520-x. Epub 2017 Aug 26.

49.

White noise speech illusion and psychosis expression: An experimental investigation of psychosis liability.

Pries LK, Guloksuz S, Menne-Lothmann C, Decoster J, van Winkel R, Collip D, Delespaul P, De Hert M, Derom C, Thiery E, Jacobs N, Wichers M, Simons CJP, Rutten BPF, van Os J.

PLoS One. 2017 Aug 23;12(8):e0183695. doi: 10.1371/journal.pone.0183695. eCollection 2017.

50.

Long-term evaluation of a hospital-based violence intervention program using a regional health information exchange.

Bell TM, Gilyan D, Moore BA, Martin J, Ogbemudia B, McLaughlin BE, Moore R, Simons CJ, Zarzaur BL.

J Trauma Acute Care Surg. 2018 Jan;84(1):175-182. doi: 10.1097/TA.0000000000001671.

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