Detalhe da pesquisa
1.
Clinical and genetic investigation of 14 families with various forms of short stature syndromes.
Clin Genet
; 2024 May 22.
Artigo
Inglês
| MEDLINE | ID: mdl-38774940
2.
Chloroplast genome evolution in the Dracunculus clade (Aroideae, Araceae).
Genomics
; 113(1 Pt 1): 183-192, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33326831
3.
Identification of a novel biallelic missense variant in the KIAA0825 underlies postaxial polydactyly type A.
Genomics
; 112(4): 2729-2733, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32147526
4.
DEADS: Depth and Energy Aware Dominating Set Based Algorithm for Cooperative Routing along with Sink Mobility in Underwater WSNs.
Sensors (Basel)
; 15(6): 14458-86, 2015 Jun 18.
Artigo
Inglês
| MEDLINE | ID: mdl-26094630
5.
A Fatigue Measuring Protocol for Wireless Body Area Sensor Networks.
J Med Syst
; 39(12): 193, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26490151
6.
Identification of a Novel Nonsense Variant in the DLL3 Gene Underlying Spondylocostal Dysostosis in a Consanguineous Pakistani Family.
Mol Syndromol
; 14(3): 191-200, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-37323197
7.
Long-term kidney transplant outcome in obese patients in a predominantly African American population.
Clin Transplant
; 25(3): E264-70, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-21332793
8.
Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance.
Mol Syndromol
; 12(6): 351-361, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34899144
9.
New-onset diabetes after hemodialysis initiation: impact on survival.
Am J Nephrol
; 31(3): 239-46, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20068288
10.
Nonsyndromic Split-Hand/Foot Malformation: Recent Classification.
Mol Syndromol
; 10(5): 243-254, 2020 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-32021595
11.
A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani family.
Clin Dysmorphol
; 29(1): 17-23, 2020 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-31469663
12.
Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation.
Genet Test Mol Biomarkers
; 24(9): 600-607, 2020 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-32762550
13.
Biallelic variants in four genes underlying recessive osteogenesis imperfecta.
Eur J Med Genet
; 63(8): 103954, 2020 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-32413570
14.
Effect of ethnicity on the progression of diabetic kidney disease independent of glycemic control.
Am J Nephrol
; 30(3): 261-7, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19494485
15.
Long-term outcomes of dual kidney transplantation-a single center experience.
Clin Transplant
; 23(3): 400-6, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19207110
16.
Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D).
Front Pediatr
; 7: 343, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31555621
17.
Posttransplant diabetes and hypertension: pathophysiologic insights and therapeutic rationale.
Curr Diab Rep
; 8(3): 221-7, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-18625120
18.
Safety issues with intravenous iron products in the management of anemia in chronic kidney disease.
Clin Med Res
; 6(3-4): 93-102, 2008 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19325171
19.
Spectrofluorimetric analysis of famotidine in pharmaceutical preparations and biological fluids by derivatization with benzoin.
Spectrochim Acta A Mol Biomol Spectrosc
; 134: 449-52, 2015 Jan 05.
Artigo
Inglês
| MEDLINE | ID: mdl-25033237
20.
Listening to patients' voices: linguistic indicators related to diabetes self-management.
Commun Med
; 9(1): 1-12, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23763232