Detalhe da pesquisa
1.
CORIN KneeTec DeepDishTM: Functional outcomes after a follow-up of 12 months and comparison with the STRYKER Triathlon PS.
Acta Orthop Belg
; 88(1): 61-71, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35512156
2.
Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis.
J Hum Genet
; 65(5): 487-491, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32015378
3.
Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome.
Am J Hum Genet
; 98(5): 971-980, 2016 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27108797
4.
[When everything is frozen, start moving again: the FIT@CHUV program]. / Quand tout est gelé, se remettre à bougerâ : programme FIT@CHUV.
Rev Med Suisse
; 15(656): 1276-1280, 2019 Jun 19.
Artigo
em Francês
| MEDLINE | ID: mdl-31268256
5.
Submicroscopic deletions at 13q32.1 cause congenital microcoria.
Am J Hum Genet
; 96(4): 631-9, 2015 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25772937
6.
Global radiological score for femoral cementless revision stem.
Int Orthop
; 42(5): 1007-1013, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28988365
7.
[Together we are stronger: management of complex functional disorders during adolescence]. / L'union fait la force :traitement des troubles fonctionnels complexes à l'adolescence.
Rev Med Suisse
; 14(603): 839-842, 2018 Apr 18.
Artigo
em Francês
| MEDLINE | ID: mdl-29668147
8.
Assessment of fixation in cementless femoral revision of total hip arthroplasty: comparison of the Engh score versus radiolucent line measurement.
Int Orthop
; 40(5): 907-12, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26572886
9.
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations.
Am J Hum Genet
; 90(5): 864-70, 2012 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22503633
10.
Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6.
Am J Hum Genet
; 90(1): 25-39, 2012 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22209248
11.
Surgical management of the infected reversed shoulder arthroplasty: a French multicenter study of reoperation in 32 patients.
J Shoulder Elbow Surg
; 24(11): 1713-22, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25957111
12.
Bone stock in revision femoral arthroplasty: a new evaluation.
Int Orthop
; 39(8): 1487-94, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25564445
13.
Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form.
Hum Genet
; 133(3): 299-310, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24142340
14.
[From congenital glaucoma to chronic open angle glaucoma in adulthood: a clinical and genetic continuum]. / Du glaucome congénital au glaucome chronique de l'adulte: un continuum clinique et génétique.
Bull Acad Natl Med
; 197(1): 133-9; discussion 140-1, 2013 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-24672985
15.
TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophy.
Am J Hum Genet
; 84(4): 493-8, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19327736
16.
Articulated bipolar vs. non-articulated conventional spacers: A comparative study of results from two-stage treatment of chronic septic arthritis in prosthetic or native hips.
Orthop Traumatol Surg Res
; 108(6): 103302, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35477037
17.
De novo design by pharmacophore-based searches in fragment spaces.
J Comput Aided Mol Des
; 25(10): 931-45, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21922280
18.
Experimental assessment of the effective friction at the base of granular chute flows on a smooth incline.
Phys Rev E
; 103(4-1): 042905, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34005905
19.
Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma.
Eur J Hum Genet
; 29(1): 131-140, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32737437
20.
Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype.
Hum Mutat
; 31(3): E1241-50, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20104588