Detalhe da pesquisa
1.
[Management of genetic renal disorders: local experience and importance of the network]. / Prise en charge des maladies rénales génétiques : expérience locale et importance du réseau.
Rev Med Suisse
; 19(832): 1245-1249, 2023 Jun 21.
Artigo
Francês
| MEDLINE | ID: mdl-37341318
2.
Increased Arterial Responsiveness to Angiotensin II in Mice Conceived by Assisted Reproductive Technologies.
Int J Mol Sci
; 23(21)2022 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36362144
3.
[Molecular genetic diagnosis in children with cochlear implants in the Western french speaking part of Switzerland]. / Diagnostic génétique moléculaire des enfants implantés cochléaires en Suisse romande.
Rev Med Suisse
; 18(798): 1855-1859, 2022 Oct 05.
Artigo
Francês
| MEDLINE | ID: mdl-36200963
4.
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients.
Hum Mutat
; 42(4): 373-377, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33492714
5.
LARS2-Perrault syndrome: a new case report and literature review.
BMC Med Genet
; 21(1): 109, 2020 05 18.
Artigo
Inglês
| MEDLINE | ID: mdl-32423379
6.
Case report: a 58 -year -old man with small kidneys and elevated liver enzymes.
BMC Nephrol
; 21(1): 107, 2020 03 27.
Artigo
Inglês
| MEDLINE | ID: mdl-32220227
7.
[Trimethylaminuriaâ : a perhaps not so uncommon case]. / Triméthylaminurieâ : un cas pas forcément si rare.
Rev Med Suisse
; 16(695): 1120-1122, 2020 May 27.
Artigo
Francês
| MEDLINE | ID: mdl-32462842
8.
[Genes and sex : which determination ?] / Entre gènes et sexe :quelle détermination ?
Rev Med Suisse
; 15(642): 596-599, 2019 Mar 13.
Artigo
Francês
| MEDLINE | ID: mdl-30865393
9.
[Preimplantation genetic testing]. / Gynécologie-obstétrique: Tests préimplantatoires de l'embryonen médecine de reproduction.
Rev Med Suisse
; 15(N° 632-633): 53-56, 2019 Jan 09.
Artigo
Francês
| MEDLINE | ID: mdl-30629370
10.
[Genetics of hearing disorders in children]. / Génétique des troubles auditifs chez l'enfant.
Rev Med Suisse
; 15(665): 1740-1745, 2019 Oct 02.
Artigo
Francês
| MEDLINE | ID: mdl-31580017
11.
Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother.
J Hum Genet
; 63(7): 847-850, 2018 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-29717186
12.
Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress.
Curr Genomics
; 19(8): 665-675, 2018 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-30532646
13.
[Intellectual disability: contribution of genetic studies to the etiological diagnosis]. / Handicap intellectuel : apport de la génétique pour le diagnostic étiologique.
Rev Med Suisse
; 14(619): 1666-1669, 2018 Sep 19.
Artigo
Francês
| MEDLINE | ID: mdl-30230775
14.
Glomerulocystic kidney disease.
Kidney Int
; 102(5): 1193, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36272745
15.
METHYLATION OF SEROTONIN RECEPTOR 3A IN ADHD, BORDERLINE PERSONALITY, AND BIPOLAR DISORDERS: LINK WITH SEVERITY OF THE DISORDERS AND CHILDHOOD MALTREATMENT.
Depress Anxiety
; 33(1): 45-55, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-26350166
16.
[Genetic kidney diseases: new perspectives on diagnosis]. / Maladies génétiques rénales: perspectives diagnostiques.
Rev Med Suisse
; 12(507): 387-8, 390-2, 2016 Feb 24.
Artigo
Francês
| MEDLINE | ID: mdl-27039603
17.
[Patients with variations of sex development : an example of interdisciplinary care]. / Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaire.
Rev Med Suisse
; 12(538): 1923-1929, 2016 Nov 09.
Artigo
Francês
| MEDLINE | ID: mdl-28696598
18.
Prevention of vascular dysfunction and arterial hypertension in mice generated by assisted reproductive technologies by addition of melatonin to culture media.
Am J Physiol Heart Circ Physiol
; 309(7): H1151-6, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26276822
19.
Recurrent spontaneous pneumothorax in an NF1 patient with a novel causative variant: broadening genotype-phenotype correlations.
BMJ Case Rep
; 17(5)2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38697680
20.
L'instinct aurait-ilune base épigénétique ?
Rev Med Suisse
; 13(571): 1441, 2017 Aug 23.
Artigo
Francês
| MEDLINE | ID: mdl-28837283