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Items: 1 to 20 of 167

1.

Outcomes after extracorporeal life support for postcardiotomy cardiogenic shock.

Pozzi M, Alvau F, Armoiry X, Grinberg D, Hugon-Vallet E, Koffel C, Portran P, Scollo G, Fellahi JL, Obadia JF.

J Card Surg. 2019 Jan 12. doi: 10.1111/jocs.13985. [Epub ahead of print]

PMID:
30636172
2.

Pro-osteoporotic miR-320a impairs osteoblast function and induces oxidative stress.

De-Ugarte L, Balcells S, Nogues X, Grinberg D, Diez-Perez A, Garcia-Giralt N.

PLoS One. 2018 Nov 28;13(11):e0208131. doi: 10.1371/journal.pone.0208131. eCollection 2018.

3.

Artificial mitral chordae: When length matters.

Grinberg D, Adamou Nouhou K, Pozzi M, Obadia JF.

J Thorac Cardiovasc Surg. 2018 Sep 29. pii: S0022-5223(18)32514-5. doi: 10.1016/j.jtcvs.2018.09.015. [Epub ahead of print] No abstract available.

PMID:
30482530
4.

Measuring chordae tension during transapical neochordae implantation: Toward understanding objective consequences of mitral valve repair.

Grinberg D, Cottinet PJ, Thivolet S, Audigier D, Capsal JF, Le MQ, Obadia JF.

J Thorac Cardiovasc Surg. 2018 Oct 17. pii: S0022-5223(18)32780-6. doi: 10.1016/j.jtcvs.2018.10.029. [Epub ahead of print]

PMID:
30454983
5.

Functional Characterization of a GGPPS Variant Identified in Atypical Femoral Fracture Patients and Delineation of the Role of GGPPS in Bone-Relevant Cell Types.

Roca-Ayats N, Ng PY, Garcia-Giralt N, Falcó-Mascaró M, Cozar M, Abril JF, Quesada Gómez JM, Prieto-Alhambra D, Nogués X, Dunford JE, Russell RG, Baron R, Grinberg D, Balcells S, Díez-Pérez A.

J Bone Miner Res. 2018 Dec;33(12):2091-2098. doi: 10.1002/jbmr.3580. Epub 2018 Sep 24.

PMID:
30184270
6.

[Clinical and molecular study in a family with multiple osteochondromatosis].

Cammarata-Scalisi F, Stock F, Avendaño A, Cozar M, Balcells S, Grinberg D.

Acta Ortop Mex. 2018 Mar-Apr;32(2):108-111. Spanish.

7.

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.

Trajanoska K, Morris JA, Oei L, Zheng HF, Evans DM, Kiel DP, Ohlsson C, Richards JB, Rivadeneira F; GEFOS/GENOMOS consortium and the 23andMe research team.

BMJ. 2018 Aug 29;362:k3225. doi: 10.1136/bmj.k3225.

8.

The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring-Opitz Syndrome.

Urreizti R, Gürsoy S, Castilla-Vallmanya L, Cunill G, Rabionet R, Erçal D, Grinberg D, Balcells S.

Clin Case Rep. 2018 Jun 10;6(8):1452-1456. doi: 10.1002/ccr3.1603. eCollection 2018 Aug.

9.

Percutaneous Repair or Medical Treatment for Secondary Mitral Regurgitation.

Obadia JF, Messika-Zeitoun D, Leurent G, Iung B, Bonnet G, Piriou N, Lefèvre T, Piot C, Rouleau F, Carrié D, Nejjari M, Ohlmann P, Leclercq F, Saint Etienne C, Teiger E, Leroux L, Karam N, Michel N, Gilard M, Donal E, Trochu JN, Cormier B, Armoiry X, Boutitie F, Maucort-Boulch D, Barnel C, Samson G, Guerin P, Vahanian A, Mewton N; MITRA-FR Investigators.

N Engl J Med. 2018 Dec 13;379(24):2297-2306. doi: 10.1056/NEJMoa1805374. Epub 2018 Aug 27.

PMID:
30145927
10.

Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density.

Martínez-Gil N, Roca-Ayats N, Monistrol-Mula A, García-Giralt N, Díez-Pérez A, Nogués X, Mellibovsky L, Grinberg D, Balcells S.

Sci Rep. 2018 Jul 19;8(1):10951. doi: 10.1038/s41598-018-29242-8.

11.

A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome.

Urreizti R, Damanti S, Esteve C, Franco-Valls H, Castilla-Vallmanya L, Tonda R, Cormand B, Vilageliu L, Opitz JM, Neri G, Grinberg D, Balcells S.

Sci Rep. 2018 Jan 12;8(1):694. doi: 10.1038/s41598-017-19109-9.

12.

Expression profiling of microRNAs in human bone tissue from postmenopausal women.

De-Ugarte L, Serra-Vinardell J, Nonell L, Balcells S, Arnal M, Nogues X, Mellibovsky L, Grinberg D, Diez-Perez A, Garcia-Giralt N.

Hum Cell. 2018 Jan;31(1):33-41. doi: 10.1007/s13577-017-0181-y. Epub 2017 Sep 20.

PMID:
28933035
13.

Correction: Stereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity.

Stauffert F, Serra-Vinardell J, Gómez-Grau M, Michelakakis H, Mavridou I, Grinberg D, Vilageliu L, Casas J, Bodlenner A, Delgado A, Compain P.

Org Biomol Chem. 2017 Sep 26;15(37):7977. doi: 10.1039/c7ob90148h.

PMID:
28905961
14.

Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease.

Herrera S, Soriano R, Nogués X, Güerri-Fernandez R, Grinberg D, García-Giralt N, Martínez-Gil N, Castejón S, González-Lizarán A, Balcells S, Diez-Perez A.

Osteoporos Int. 2017 Dec;28(12):3489-3493. doi: 10.1007/s00198-017-4198-6. Epub 2017 Aug 25.

PMID:
28842728
15.

High rate of arterial complications in patients supported with extracorporeal life support for drug intoxication-induced refractory cardiogenic shock or cardiac arrest.

Pozzi M, Koffel C, Djaref C, Grinberg D, Fellahi JL, Hugon-Vallet E, Prieur C, Robin J, Obadia JF.

J Thorac Dis. 2017 Jul;9(7):1988-1996. doi: 10.21037/jtd.2017.06.81.

16.

Erratum to: MiRNA profiling of whole trabecular bone: identification of osteoporosis-related changes in MiRNAs in human hip bones.

De-Ugarte L, Yoskovitz G, Balcells S, Güerri-Fernández R, Martinez-Diaz S, Mellibovsky L, Urreizti R, Nogués X, Grinberg D, García-Giralt N, Díez-Pérez A.

BMC Med Genomics. 2017 May 23;10(1):36. doi: 10.1186/s12920-017-0272-3. No abstract available.

17.

GGPS1 Mutation and Atypical Femoral Fractures with Bisphosphonates.

Roca-Ayats N, Balcells S, Garcia-Giralt N, Falcó-Mascaró M, Martínez-Gil N, Abril JF, Urreizti R, Dopazo J, Quesada-Gómez JM, Nogués X, Mellibovsky L, Prieto-Alhambra D, Dunford JE, Javaid MK, Russell RG, Grinberg D, Díez-Pérez A.

N Engl J Med. 2017 May 4;376(18):1794-1795. doi: 10.1056/NEJMc1612804. No abstract available.

PMID:
28467865
18.

Stereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity.

Stauffert F, Serra-Vinardell J, Gómez-Grau M, Michelakakis H, Mavridou I, Grinberg D, Vilageliu L, Casas J, Bodlenner A, Delgado A, Compain P.

Org Biomol Chem. 2017 May 3;15(17):3681-3705. doi: 10.1039/c7ob00443e.

PMID:
28401966
19.

A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.

Urreizti R, Cueto-Gonzalez AM, Franco-Valls H, Mort-Farre S, Roca-Ayats N, Ponomarenko J, Cozzuto L, Company C, Bosio M, Ossowski S, Montfort M, Hecht J, Tizzano EF, Cormand B, Vilageliu L, Opitz JM, Neri G, Grinberg D, Balcells S.

Sci Rep. 2017 Mar 10;7:44138. doi: 10.1038/srep44138.

20.

New murine Niemann-Pick type C models bearing a pseudoexon-generating mutation recapitulate the main neurobehavioural and molecular features of the disease.

Gómez-Grau M, Albaigès J, Casas J, Auladell C, Dierssen M, Vilageliu L, Grinberg D.

Sci Rep. 2017 Feb 7;7:41931. doi: 10.1038/srep41931.

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