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Items: 1 to 50 of 180

1.

The role of deformability in determining the structural and mechanical properties of bubbles and emulsions.

Boromand A, Signoriello A, Lowensohn J, Orellana CS, Weeks ER, Ye F, Shattuck MD, O'Hern CS.

Soft Matter. 2019 Jul 24;15(29):5854-5865. doi: 10.1039/c9sm00775j.

PMID:
31246221
2.

The Use of Dynamic Assessment for the Diagnosis of Language Disorders in Bilingual Children: A Meta-Analysis.

Orellana CI, Wada R, Gillam RB.

Am J Speech Lang Pathol. 2019 Aug 9;28(3):1298-1317. doi: 10.1044/2019_AJSLP-18-0202. Epub 2019 Jun 13.

PMID:
31194570
3.

Precarious employment and mental health: a systematic review and meta-analysis of longitudinal studies.

Rönnblad T, Grönholm E, Jonsson J, Koranyi I, Orellana C, Kreshpaj B, Chen L, Stockfelt L, Bodin T.

Scand J Work Environ Health. 2019 Jan 25. pii: 3797. doi: 10.5271/sjweh.3797. [Epub ahead of print]

4.

Revisiting the Evolution and Taxonomy of Clostridia, a Phylogenomic Update.

Cruz-Morales P, Orellana CA, Moutafis G, Moonen G, Rincon G, Nielsen LK, Marcellin E.

Genome Biol Evol. 2019 Jul 1;11(7):2035-2044. doi: 10.1093/gbe/evz096.

5.

Precarious employment, business performance and occupational injuries: a study protocol of a register-based Swedish project.

Orellana C, Kreshpaj B, Johansson G, Burström B, Kjellberg K, Hemmingsson T, Axén M, Davis L, Wegman D, Bodin T.

BMJ Open. 2019 Feb 19;9(2):e026091. doi: 10.1136/bmjopen-2018-026091.

6.

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

van der Sluijs PJ, Jansen S, Vergano SA, Adachi-Fukuda M, Alanay Y, AlKindy A, Baban A, Bayat A, Beck-Wödl S, Berry K, Bijlsma EK, Bok LA, Brouwer AFJ, van der Burgt I, Campeau PM, Canham N, Chrzanowska K, Chu YWY, Chung BHY, Dahan K, De Rademaeker M, Destree A, Dudding-Byth T, Earl R, Elcioglu N, Elias ER, Fagerberg C, Gardham A, Gener B, Gerkes EH, Grasshoff U, van Haeringen A, Heitink KR, Herkert JC, den Hollander NS, Horn D, Hunt D, Kant SG, Kato M, Kayserili H, Kersseboom R, Kilic E, Krajewska-Walasek M, Lammers K, Laulund LW, Lederer D, Lees M, López-González V, Maas S, Mancini GMS, Marcelis C, Martinez F, Maystadt I, McGuire M, McKee S, Mehta S, Metcalfe K, Milunsky J, Mizuno S, Moeschler JB, Netzer C, Ockeloen CW, Oehl-Jaschkowitz B, Okamoto N, Olminkhof SNM, Orellana C, Pasquier L, Pottinger C, Riehmer V, Robertson SP, Roifman M, Rooryck C, Ropers FG, Rosello M, Ruivenkamp CAL, Sagiroglu MS, Sallevelt SCEH, Calvo AS, Simsek-Kiper PO, Soares G, Solaeche L, Sonmez FM, Splitt M, Steenbeek D, Stegmann APA, Stumpel CTRM, Tanabe S, Uctepe E, Utine GE, Veenstra-Knol HE, Venkateswaran S, Vilain C, Vincent-Delorme C, Vulto-van Silfhout AT, Wheeler P, Wilson GN, Wilson LC, Wollnik B, Kosho T, Wieczorek D, Eichler E, Pfundt R, de Vries BBA, Clayton-Smith J, Santen GWE.

Genet Med. 2019 Jan 29. doi: 10.1038/s41436-018-0368-y. [Epub ahead of print]

PMID:
30696996
7.

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.

Machol K, Rousseau J, Ehresmann S, Garcia T, Nguyen TTM, Spillmann RC, Sullivan JA, Shashi V, Jiang YH, Stong N, Fiala E, Willing M, Pfundt R, Kleefstra T, Cho MT, McLaughlin H, Rosello Piera M, Orellana C, Martínez F, Caro-Llopis A, Monfort S, Roscioli T, Nixon CY, Buckley MF, Turner A, Jones WD, van Hasselt PM, Hofstede FC, van Gassen KLI, Brooks AS, van Slegtenhorst MA, Lachlan K, Sebastian J, Madan-Khetarpal S, Sonal D, Sakkubai N, Thevenon J, Faivre L, Maurel A, Petrovski S, Krantz ID, Tarpinian JM, Rosenfeld JA, Lee BH; Undiagnosed Diseases Network, Campeau PM.

Am J Hum Genet. 2019 Jan 3;104(1):164-178. doi: 10.1016/j.ajhg.2018.11.007. Epub 2018 Dec 20.

8.

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

van der Sluijs PJ, Jansen S, Vergano SA, Adachi-Fukuda M, Alanay Y, AlKindy A, Baban A, Bayat A, Beck-Wödl S, Berry K, Bijlsma EK, Bok LA, Brouwer AFJ, van der Burgt I, Campeau PM, Canham N, Chrzanowska K, Chu YWY, Chung BHY, Dahan K, De Rademaeker M, Destree A, Dudding-Byth T, Earl R, Elcioglu N, Elias ER, Fagerberg C, Gardham A, Gener B, Gerkes EH, Grasshoff U, van Haeringen A, Heitink KR, Herkert JC, den Hollander NS, Horn D, Hunt D, Kant SG, Kato M, Kayserili H, Kersseboom R, Kilic E, Krajewska-Walasek M, Lammers K, Laulund LW, Lederer D, Lees M, López-González V, Maas S, Mancini GMS, Marcelis C, Martinez F, Maystadt I, McGuire M, McKee S, Mehta S, Metcalfe K, Milunsky J, Mizuno S, Moeschler JB, Netzer C, Ockeloen CW, Oehl-Jaschkowitz B, Okamoto N, Olminkhof SNM, Orellana C, Pasquier L, Pottinger C, Riehmer V, Robertson SP, Roifman M, Rooryck C, Ropers FG, Rosello M, Ruivenkamp CAL, Sagiroglu MS, Sallevelt SCEH, Sanchis Calvo A, Simsek-Kiper PO, Soares G, Solaeche L, Sonmez FM, Splitt M, Steenbeek D, Stegmann APA, Stumpel CTRM, Tanabe S, Uctepe E, Utine GE, Veenstra-Knol HE, Venkateswaran S, Vilain C, Vincent-Delorme C, Vulto-van Silfhout AT, Wheeler P, Wilson GN, Wilson LC, Wollnik B, Kosho T, Wieczorek D, Eichler E, Pfundt R, de Vries BBA, Clayton-Smith J, Santen GWE.

Genet Med. 2019 Jun;21(6):1295-1307. doi: 10.1038/s41436-018-0330-z. Epub 2018 Nov 8. Erratum in: Genet Med. 2019 Jan 29;:.

PMID:
30349098
9.

A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism.

D Hidalgo-Santos A, Del Carmen DeMingo-Alemany M, Moreno-Macián F, Roselló M, Orellana C, Martínez F, Caro-Llopis A, León-Cariñena S, Tomás-Vila M.

Int J Endocrinol Metab. 2018 Jul 1;16(3):e67329. doi: 10.5812/ijem.67329. eCollection 2018 Jul.

10.

Influence of HLA-B27 on the Ankylosing Spondylitis phenotype: results from the REGISPONSER database.

Arévalo M, Gratacós Masmitjà J, Moreno M, Calvet J, Orellana C, Ruiz D, Castro C, Carreto P, Larrosa M, Collantes E, Font P; REGISPONSER group.

Arthritis Res Ther. 2018 Oct 3;20(1):221. doi: 10.1186/s13075-018-1724-7.

11.

Ultrasound Findings in Patients With Femoracetabular Impingement Without Radiographic Osteoarthritis: A Pilot Study.

Orellana C, Moreno M, Calvet J, Navarro N, García-Manrique M, Gratacós J.

J Ultrasound Med. 2019 Apr;38(4):895-901. doi: 10.1002/jum.14768. Epub 2018 Sep 11.

PMID:
30203593
12.

Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.

Hemati P, Revah-Politi A, Bassan H, Petrovski S, Bilancia CG, Ramsey K, Griffin NG, Bier L, Cho MT, Rosello M, Lynch SA, Colombo S, Weber A, Haug M, Heinzen EL, Sands TT, Narayanan V, Primiano M, Aggarwal VS, Millan F, Sattler-Holtrop SG, Caro-Llopis A, Pillar N, Baker J, Freedman R, Kroes HY, Sacharow S, Stong N, Lapunzina P, Schneider MC, Mendelsohn NJ, Singleton A, Loik Ramey V, Wou K, Kuzminsky A, Monfort S, Weiss M, Doyle S, Iglesias A, Martinez F, Mckenzie F, Orellana C, van Gassen KLI, Palomares M, Bazak L, Lee A, Bircher A, Basel-Vanagaite L, Hafström M, Houge G; C4RCD Research Group; DDD study, Goldstein DB, Anyane-Yeboa K.

Am J Med Genet A. 2018 Nov;176(11):2259-2275. doi: 10.1002/ajmg.a.40472. Epub 2018 Sep 8.

PMID:
30194818
13.

De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.

Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, Bruel AL, Buchert R, Calpena E, Cogné B, Dallapiccola B, Distelmaier F, Elmslie F, Faivre L, Haack TB, Harrison V, Henderson A, Hunt D, Isidor B, Joset P, Kumada S, Lachmeijer AMA, Lees M, Lynch SA, Martinez F, Matsumoto N, McDougall C, Mefford HC, Miyake N, Myers CT, Moutton S, Nesbitt A, Novelli A, Orellana C, Rauch A, Rosello M, Saida K, Santani AB, Sarkar A, Scheffer IE, Shinawi M, Steindl K, Symonds JD, Zackai EH; University of Washington Center for Mendelian Genomics; DDD Study, Reis A, Sticht H, Zweier C.

Am J Hum Genet. 2018 Aug 2;103(2):305-316. doi: 10.1016/j.ajhg.2018.07.003. Epub 2018 Jul 26.

14.

Clinical and ultrasonographic features associated to response to intraarticular corticosteroid injection. A one year follow up prospective cohort study in knee osteoarthritis patient with joint effusion.

Calvet J, Orellana C, Galisteo C, García-Manrique M, Navarro N, Caixàs A, Larrosa M, Gratacós J.

PLoS One. 2018 Jan 19;13(1):e0191342. doi: 10.1371/journal.pone.0191342. eCollection 2018.

15.

RNA-Seq Highlights High Clonal Variation in Monoclonal Antibody Producing CHO Cells.

Orellana CA, Marcellin E, Palfreyman RW, Munro TP, Gray PP, Nielsen LK.

Biotechnol J. 2018 Mar;13(3):e1700231. doi: 10.1002/biot.201700231. Epub 2018 Feb 1.

PMID:
29316330
16.

Differential involvement of synovial adipokines in pain and physical function in female patients with knee osteoarthritis. A cross-sectional study.

Calvet J, Orellana C, Albiñana Giménez N, Berenguer-Llergo A, Caixàs A, García-Manrique M, Galisteo Lencastre C, Navarro N, Larrosa M, Gratacós J.

Osteoarthritis Cartilage. 2018 Feb;26(2):276-284. doi: 10.1016/j.joca.2017.11.010. Epub 2017 Nov 28.

17.

Oral contraceptives, breastfeeding and the risk of developing rheumatoid arthritis: results from the Swedish EIRA study.

Orellana C, Saevarsdottir S, Klareskog L, Karlson EW, Alfredsson L, Bengtsson C.

Ann Rheum Dis. 2017 Nov;76(11):1845-1852. doi: 10.1136/annrheumdis-2017-211620. Epub 2017 Aug 17.

18.

Imageability ratings across languages.

Rofes A, Zakariás L, Ceder K, Lind M, Johansson MB, de Aguiar V, Bjekić J, Fyndanis V, Gavarró A, Simonsen HG, Sacristán CH, Kambanaros M, Kraljević JK, Martínez-Ferreiro S, Mavis İ, Orellana CM, Sör I, Lukács Á, Tunçer M, Vuksanović J, Ibarrola AM, Pourquie M, Varlokosta S, Howard D.

Behav Res Methods. 2018 Jun;50(3):1187-1197. doi: 10.3758/s13428-017-0936-0.

PMID:
28707216
19.

Chimeric Genes in Deletions and Duplications Associated with Intellectual Disability.

Mayo S, Monfort S, Roselló M, Orellana C, Oltra S, Caro-Llopis A, Martínez F.

Int J Genomics. 2017;2017:4798474. doi: 10.1155/2017/4798474. Epub 2017 May 24.

20.

[Epidemiology of premature deaths in Chile between 2001 and 2010].

Bächler R, Icaza G, Soto A, Núñez L, Orellana C, Monsalve R, Riquelme M.

Rev Med Chil. 2017 Mar;145(3):319-326. doi: 10.4067/S0034-98872017000300005. Spanish.

21.

[Effectiveness of a structured educative program in Chilean diabetic patients].

Bächler R, Mujica V, Orellana C, Cáceres D, Carrasco N, Davidson C, Jiménez AL, Luna P, Valladares E, Vergara A.

Rev Med Chil. 2017 Feb;145(2):181-187. doi: 10.4067/S0034-98872017000200005. Spanish.

22.

Overexpression of the regulatory subunit of glutamate-cysteine ligase enhances monoclonal antibody production in CHO cells.

Orellana CA, Marcellin E, Gray PP, Nielsen LK.

Biotechnol Bioeng. 2017 Aug;114(8):1825-1836. doi: 10.1002/bit.26316. Epub 2017 May 8.

PMID:
28436007
23.

Generation of a disease-specific iPS cell line derived from a patient with Charcot-Marie-Tooth type 2K lacking functional GDAP1 gene.

Martí S, León M, Orellana C, Prieto J, Ponsoda X, López-García C, Vílchez JJ, Sevilla T, Torres J.

Stem Cell Res. 2017 Jan;18:1-4. doi: 10.1016/j.scr.2016.11.017. Epub 2016 Dec 2.

24.

Effect of chondroitin sulphate on synovitis of knee osteoarthritic patients.

Tío L, Orellana C, Pérez-García S, Piqueras L, Escudero P, Juarranz Y, Garcia-Giralt N, Montañés F, Farran A, Benito P, Gomariz RP, Sanz MJ, Monfort J.

Med Clin (Barc). 2017 Jul 7;149(1):9-16. doi: 10.1016/j.medcli.2016.12.045. Epub 2017 Feb 27. English, Spanish.

PMID:
28245911
25.

Association Between Menopausal Factors and the Risk of Seronegative and Seropositive Rheumatoid Arthritis: Results From the Nurses' Health Studies.

Bengtsson C, Malspeis S, Orellana C, Sparks JA, Costenbader KH, Karlson EW.

Arthritis Care Res (Hoboken). 2017 Nov;69(11):1676-1684. doi: 10.1002/acr.23194. Epub 2017 Sep 21.

26.

A Consensus Genome-scale Reconstruction of Chinese Hamster Ovary Cell Metabolism.

Hefzi H, Ang KS, Hanscho M, Bordbar A, Ruckerbauer D, Lakshmanan M, Orellana CA, Baycin-Hizal D, Huang Y, Ley D, Martinez VS, Kyriakopoulos S, Jiménez NE, Zielinski DC, Quek LE, Wulff T, Arnsdorf J, Li S, Lee JS, Paglia G, Loira N, Spahn PN, Pedersen LE, Gutierrez JM, King ZA, Lund AM, Nagarajan H, Thomas A, Abdel-Haleem AM, Zanghellini J, Kildegaard HF, Voldborg BG, Gerdtzen ZP, Betenbaugh MJ, Palsson BO, Andersen MR, Nielsen LK, Borth N, Lee DY, Lewis NE.

Cell Syst. 2016 Nov 23;3(5):434-443.e8. doi: 10.1016/j.cels.2016.10.020.

27.

Synovial fluid adipokines are associated with clinical severity in knee osteoarthritis: a cross-sectional study in female patients with joint effusion.

Calvet J, Orellana C, Gratacós J, Berenguer-Llergo A, Caixàs A, Chillarón JJ, Pedro-Botet J, García-Manrique M, Navarro N, Larrosa M.

Arthritis Res Ther. 2016 Sep 15;18(1):207. doi: 10.1186/s13075-016-1103-1.

28.

High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing.

Martínez F, Caro-Llopis A, Roselló M, Oltra S, Mayo S, Monfort S, Orellana C.

J Med Genet. 2017 Feb;54(2):87-92. doi: 10.1136/jmedgenet-2016-103964. Epub 2016 Sep 12.

PMID:
27620904
29.

Metabolic Reconstruction of Setaria italica: A Systems Biology Approach for Integrating Tissue-Specific Omics and Pathway Analysis of Bioenergy Grasses.

de Oliveira Dal'Molin CG, Orellana C, Gebbie L, Steen J, Hodson MP, Chrysanthopoulos P, Plan MR, McQualter R, Palfreyman RW, Nielsen LK.

Front Plant Sci. 2016 Aug 10;7:1138. doi: 10.3389/fpls.2016.01138. eCollection 2016.

30.

De novo mutations in genes of mediator complex causing syndromic intellectual disability: mediatorpathy or transcriptomopathy?

Caro-Llopis A, Rosello M, Orellana C, Oltra S, Monfort S, Mayo S, Martinez F.

Pediatr Res. 2016 Dec;80(6):809-815. doi: 10.1038/pr.2016.162. Epub 2016 Aug 8.

PMID:
27500536
31.

Recon 2.2: from reconstruction to model of human metabolism.

Swainston N, Smallbone K, Hefzi H, Dobson PD, Brewer J, Hanscho M, Zielinski DC, Ang KS, Gardiner NJ, Gutierrez JM, Kyriakopoulos S, Lakshmanan M, Li S, Liu JK, Martínez VS, Orellana CA, Quek LE, Thomas A, Zanghellini J, Borth N, Lee DY, Nielsen LK, Kell DB, Lewis NE, Mendes P.

Metabolomics. 2016;12:109. Epub 2016 Jun 7.

32.

Occupational exposure to polycyclic aromatic hydrocarbons: A cross-sectional study in bars and restaurants in Santiago, Chile.

Muñoz C, Droppelmann A, Erazo M, Aceituno P, Orellana C, Parro J, Mesias S, Marchetti N, Navas-Acien A, Iglesias V.

Am J Ind Med. 2016 Oct;59(10):887-96. doi: 10.1002/ajim.22616. Epub 2016 Jun 27.

33.

Multi-year optimization of malaria intervention: a mathematical model.

Dudley HJ, Goenka A, Orellana CJ, Martonosi SE.

Malar J. 2016 Mar 1;15:133. doi: 10.1186/s12936-016-1182-0.

34.

Improvement of photovoltaic performance by substituent effect of donor and acceptor structure of TPA-based dye-sensitized solar cells.

Inostroza N, Mendizabal F, Arratia-Pérez R, Orellana C, Linares-Flores C.

J Mol Model. 2016 Jan;22(1):25. doi: 10.1007/s00894-015-2893-9. Epub 2016 Jan 7.

PMID:
26744295
35.

Measuring Global Brain Atrophy with the Brain Volume/Cerebrospinal Fluid Index: Normative Values, Cut-Offs and Clinical Associations.

Orellana C, Ferreira D, Muehlboeck JS, Mecocci P, Vellas B, Tsolaki M, Kłoszewska I, Soininen H, Lovestone S, Simmons A, Wahlund LO, Westman E; AddNeuronMed consortium and for the Alzheimer''s Disease Neuroimaging Initiative.

Neurodegener Dis. 2016;16(1-2):77-86. doi: 10.1159/000442443. Epub 2015 Dec 19.

PMID:
26726737
36.

Parity influences the severity of ACPA-negative early rheumatoid arthritis: a cohort study based on the Swedish EIRA material.

Pikwer M, Orellana C, Källberg H, Pikwer A, Turesson C, Klareskog L, Alfredsson L, Saevarsdottir S, Bengtsson C.

Arthritis Res Ther. 2015 Dec 12;17:358. doi: 10.1186/s13075-015-0869-x.

37.

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.

O'Rawe JA, Wu Y, Dörfel MJ, Rope AF, Au PY, Parboosingh JS, Moon S, Kousi M, Kosma K, Smith CS, Tzetis M, Schuette JL, Hufnagel RB, Prada CE, Martinez F, Orellana C, Crain J, Caro-Llopis A, Oltra S, Monfort S, Jiménez-Barrón LT, Swensen J, Ellingwood S, Smith R, Fang H, Ospina S, Stegmann S, Den Hollander N, Mittelman D, Highnam G, Robison R, Yang E, Faivre L, Roubertie A, Rivière JB, Monaghan KG, Wang K, Davis EE, Katsanis N, Kalscheuer VM, Wang EH, Metcalfe K, Kleefstra T, Innes AM, Kitsiou-Tzeli S, Rosello M, Keegan CE, Lyon GJ.

Am J Hum Genet. 2015 Dec 3;97(6):922-32. doi: 10.1016/j.ajhg.2015.11.005.

38.

High prevalence of cardiovascular co-morbidities in patients with symptomatic knee or hand osteoarthritis.

Calvet J, Orellana C, Larrosa M, Navarro N, Chillarón JJ, Pedro-Botet J, Galisteo C, García-Manrique M, Gratacós J.

Scand J Rheumatol. 2016 Jan;45(1):41-44. doi: 10.3109/03009742.2015.1054875. Epub 2015 Aug 31.

PMID:
26312543
39.

Haploinsufficiency of the MYT1L gene causes intellectual disability frequently associated with behavioral disorder.

Mayo S, Roselló M, Monfort S, Oltra S, Orellana C, Martínez F.

Genet Med. 2015 Aug;17(8):683-4. doi: 10.1038/gim.2015.86. No abstract available.

PMID:
26240977
40.

Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes.

Martinez F, Marín-Reina P, Sanchis-Calvo A, Perez-Aytés A, Oltra S, Roselló M, Mayo S, Monfort S, Pantoja J, Orellana C.

Pediatr Res. 2015 Nov;78(5):533-9. doi: 10.1038/pr.2015.135. Epub 2015 Jul 22.

PMID:
26200704
41.

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients.

Mayo S, Monfort S, Roselló M, Oltra S, Orellana C, Martínez F.

Biomed Res Int. 2015;2015:341986. doi: 10.1155/2015/341986. Epub 2015 May 27.

42.

Multi-system involvement in a severe variant of fibrodysplasia ossificans progressiva (ACVR1 c.772G>A; R258G): A report of two patients.

Kaplan FS, Kobori JA, Orellana C, Calvo I, Rosello M, Martinez F, Lopez B, Xu M, Pignolo RJ, Shore EM, Groppe JC.

Am J Med Genet A. 2015 Oct;167A(10):2265-71. doi: 10.1002/ajmg.a.37205. Epub 2015 Jun 11.

43.

A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next-generation sequencing causes CK syndrome.

Preiksaitiene E, Caro A, Benušienė E, Oltra S, Orellana C, Morkūnienė A, Roselló MP, Kasnauskiene J, Monfort S, Kučinskas V, Mayo S, Martinez F.

Am J Med Genet A. 2015 Jun;167(6):1342-8. doi: 10.1002/ajmg.a.36999. Epub 2015 Apr 21.

PMID:
25900314
44.

Pure duplication of 19p13.3 in three members of a family with intellectual disability and literature review. Definition of a new microduplication syndrome.

Orellana C, Roselló M, Monfort S, Mayo S, Oltra S, Martínez F.

Am J Med Genet A. 2015 Jul;167(7):1614-20. doi: 10.1002/ajmg.a.37046. Epub 2015 Apr 9. Review.

PMID:
25858326
45.

Postmenopausal hormone therapy and the risk of rheumatoid arthritis: results from the Swedish EIRA population-based case-control study.

Orellana C, Saevarsdottir S, Klareskog L, Karlson EW, Alfredsson L, Bengtsson C.

Eur J Epidemiol. 2015 May;30(5):449-57. doi: 10.1007/s10654-015-0004-y. Epub 2015 Mar 12.

46.

Infectious and immunologic phenotype of MECP2 duplication syndrome.

Bauer M, Kölsch U, Krüger R, Unterwalder N, Hameister K, Kaiser FM, Vignoli A, Rossi R, Botella MP, Budisteanu M, Rosello M, Orellana C, Tejada MI, Papuc SM, Patat O, Julia S, Touraine R, Gomes T, Wenner K, Xu X, Afenjar A, Toutain A, Philip N, Jezela-Stanek A, Gortner L, Martinez F, Echenne B, Wahn V, Meisel C, Wieczorek D, El-Chehadeh S, Van Esch H, von Bernuth H.

J Clin Immunol. 2015 Feb;35(2):168-81. doi: 10.1007/s10875-015-0129-5. Epub 2015 Feb 27.

PMID:
25721700
47.

Improved prediction of knee osteoarthritis progression by genetic polymorphisms: the Arthrotest Study.

Blanco FJ, Möller I, Romera M, Rozadilla A, Sánchez-Lázaro JA, Rodríguez A, Gálvez J, Forés J, Monfort J, Ojeda S, Moragues C, Caracuel MÁ, Clavaguera T, Valdés C, Soler JM, Orellana C, Belmonte MÁ, Martín F, Giménez S, Úcar E, Pous J, Bartolomé N, Artieda M, Szczypiorska M, Tejedor D, Martínez A, Montell E, Martínez H, Herrero M, Vergés J; Arthrotest Study Group.

Rheumatology (Oxford). 2015 Jul;54(7):1236-43. doi: 10.1093/rheumatology/keu478. Epub 2015 Jan 7.

PMID:
25573839
48.

Malignant phyllodes tumor of the breast presenting with hypoglycemia: a case report and literature review.

Pacioles T, Seth R, Orellana C, John I, Panuganty V, Dhaliwal R.

Cancer Manag Res. 2014 Dec 8;6:467-73. doi: 10.2147/CMAR.S71933. eCollection 2014.

49.

High-antibody-producing Chinese hamster ovary cells up-regulate intracellular protein transport and glutathione synthesis.

Orellana CA, Marcellin E, Schulz BL, Nouwens AS, Gray PP, Nielsen LK.

J Proteome Res. 2015 Feb 6;14(2):609-18. doi: 10.1021/pr501027c. Epub 2015 Jan 14.

PMID:
25495469
50.

Comparative efficacy of intra-articular hyaluronic acid and corticoid injections in osteoarthritis of the first carpometacarpal joint: results of a 6-month single-masked randomized study.

Monfort J, Rotés-Sala D, Segalés N, Montañes FJ, Orellana C, Llorente-Onaindia J, Mojal S, Padró I, Benito P.

Joint Bone Spine. 2015 Mar;82(2):116-21. doi: 10.1016/j.jbspin.2014.08.008. Epub 2014 Oct 11.

PMID:
25311256

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