Works matching IS 15524868 AND DT 2022 AND VI 190 AND IP 3

Results: 17

Introduction to special issue for kidney genetics.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 261, doi. 10.1002/ajmg.c.32011
Publication type:: Article

The growing power of Kidney Genetics.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 262, doi. 10.1002/ajmg.c.32010
Publication type:: Article

Genetic diagnosis and renal biopsy findings in the setting of a renal genetics clinic.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 302, doi. 10.1002/ajmg.c.32009

By:

Ben Moshe, Yishay;
Bekheirnia, Nasim;
Smith, Richard J. H.;
Hicks, John;
Braun, Michael C.;
Bekheirnia, Mir Reza

Publication type:

Article

Autosomal dominant tubulointerstitial kidney disease: A review.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 309, doi. 10.1002/ajmg.c.32008

By:

Živná, Martina;
Kidd, Kendrah O.;
Barešová, Veronika;
Hůlková, Helena;
Kmoch, Stanislav;
Bleyer, Anthony J.

Publication type:

Article

Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 325, doi. 10.1002/ajmg.c.32006

By:

Connaughton, Dervla M.;
Hildebrandt, Friedhelm

Publication type:

Article

Incorporating genetics services into adult kidney disease care.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 289, doi. 10.1002/ajmg.c.32004

By:

Bogyo, Kelsie;
Vena, Natalie;
May, Halie;
Rasouly, Hila Milo;
Marasa, Maddalena;
Sanna‐Cherchi, Simone;
Kiryluk, Krzysztof;
Nestor, Jordan;
Gharavi, Ali

Publication type:

Article

C3 glomerulopathy: Understanding an ultra‐rare complement‐mediated renal disease.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 344, doi. 10.1002/ajmg.c.31986

By:

Heiderscheit, Amanda K.;
Hauer, Jill J.;
Smith, Richard J. H.

Publication type:

Article

Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 358, doi. 10.1002/ajmg.c.31995

By:

Claus, Laura R.;
Snoek, Rozemarijn;
Knoers, Nine V. A. M.;
van Eerde, Albertien M.

Publication type:

Article

Systematic assessment of monogenic etiology in adult‐onset kidney stone formers undergoing urological intervention–evidence for genetic pretest probability.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 279, doi. 10.1002/ajmg.c.31991

By:

Schönauer, Ria;
Scherer, Lotte;
Nemitz‐Kliemchen, Melanie;
Hagemann, Tobias;
Hantmann, Elena;
Seidel, Anna;
Müller, Luise;
Kehr, Stephanie;
Voigt, Cornelia;
Stolzenburg, Jens‐Uwe;
Halbritter, Jan

Publication type:

Article

Monogenic focal segmental glomerulosclerosis: A conceptual framework for identification and management of a heterogeneous disease.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 377, doi. 10.1002/ajmg.c.31990

By:

Sambharia, Meenakshi;
Rastogi, Prerna;
Thomas, Christie P.

Publication type:

Article

Publication schedule for 2022.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 259, doi. 10.1002/ajmg.c.31925
Publication type:: Article

Pallister‐Hall syndrome, GLI3, and kidney malformation.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 264, doi. 10.1002/ajmg.c.31999

By:

McClelland, Kathryn;
Li, Weili;
Rosenblum, Norman D.

Publication type:

Article

Corrigendum Neurocutaneous syndromes in Art and Antiquities. Am J Med Genet C. 2021;187(3):349–356. Doi:10.1002/ajmg.c.31915″.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 405, doi. 10.1002/ajmg.c.31971
Publication type:: Article

Corrigendum Neurocutaneous syndromes in Art and Antiquities. Am J Med Genet C. 2021;187(2):224–234. Doi:10.1002/ajmg.c.31917.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 404, doi. 10.1002/ajmg.c.31961
Publication type:: Article

Cover Image, Volume 190, Number 3, September 2022.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. i, doi. 10.1002/ajmg.c.31926
Publication type:: Article

Genetic testing and glomerular hematuria—A nephrologist's perspective.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 399, doi. 10.1002/ajmg.c.31987
Publication type:: Article

Table of Contents, Volume 190, Number 3, September 2022.

Published in:: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 3, p. 257, doi. 10.1002/ajmg.c.31924
Publication type:: Article