Pesquisa | Biblioteca Virtual em Saúde

1.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon, D B; Karet, F E; Rodriguez-Soriano, J; Hamdan, J H; DiPietro, A; Trachtman, H; Sanjad, S A; Lifton, R P.

Nat Genet ; 14(2): 152-6, 1996 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-8841184

2.

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.

Simon, D B; Karet, F E; Hamdan, J M; DiPietro, A; Sanjad, S A; Lifton, R P.

Nat Genet ; 13(2): 183-8, 1996 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-8640224

3.

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Simon, D B; Nelson-Williams, C; Bia, M J; Ellison, D; Karet, F E; Molina, A M; Vaara, I; Iwata, F; Cushner, H M; Koolen, M; Gainza, F J; Gitleman, H J; Lifton, R P.

Nat Genet ; 12(1): 24-30, 1996 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-8528245

4.

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.

Mansfield, T A; Simon, D B; Farfel, Z; Bia, M; Tucci, J R; Lebel, M; Gutkin, M; Vialettes, B; Christofilis, M A; Kauppinen-Makelin, R; Mayan, H; Risch, N; Lifton, R P.

Nat Genet ; 16(2): 202-5, 1997 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-9171836

5.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon, D B; Bindra, R S; Mansfield, T A; Nelson-Williams, C; Mendonca, E; Stone, R; Schurman, S; Nayir, A; Alpay, H; Bakkaloglu, A; Rodriguez-Soriano, J; Morales, J M; Sanjad, S A; Taylor, C M; Pilz, D; Brem, A; Trachtman, H; Griswold, W; Richard, G A; John, E; Lifton, R P.

Nat Genet ; 17(2): 171-8, 1997 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-9326936

6.

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

Simon, D B; Lifton, R P.

Curr Opin Cell Biol ; 10(4): 450-4, 1998 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-9719864

7.

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Simon, D B; Lu, Y; Choate, K A; Velazquez, H; Al-Sabban, E; Praga, M; Casari, G; Bettinelli, A; Colussi, G; Rodriguez-Soriano, J; McCredie, D; Milford, D; Sanjad, S; Lifton, R P.

Science ; 285(5424): 103-6, 1999 Jul 02.

Artigo em Inglês | MEDLINE | ID: mdl-10390358

8.

Human hypertension caused by mutations in WNK kinases.

Wilson, F H; Disse-Nicodème, S; Choate, K A; Ishikawa, K; Nelson-Williams, C; Desitter, I; Gunel, M; Milford, D V; Lipkin, G W; Achard, J M; Feely, M P; Dussol, B; Berland, Y; Unwin, R J; Mayan, H; Simon, D B; Farfel, Z; Jeunemaitre, X; Lifton, R P.

Science ; 293(5532): 1107-12, 2001 Aug 10.

Artigo em Inglês | MEDLINE | ID: mdl-11498583

9.

The role of Cas8 in type I CRISPR interference.

Cass, Simon D B; Haas, Karina A; Stoll, Britta; Alkhnbashi, Omer S; Sharma, Kundan; Urlaub, Henning; Backofen, Rolf; Marchfelder, Anita; Bolt, Edward L.

Biosci Rep ; 35(3)2015 May 05.

Artigo em Inglês | MEDLINE | ID: mdl-26182359

10.

Symptomatic osseous sarcoidosis with findings on bone scan.

Silver, H M; Shirkhoda, A; Simon, D B.

Chest ; 73(2): 238-41, 1978 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-145934

11.

Unusual causes of stroke in a young adult.

Newman, P E; Simon, D B; Law, R K; Earnest, M P.

Arch Intern Med ; 140(11): 1502-3, 1980 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-7436646

12.

Luetic meningitis with gumma.

Simon, D B.

Neurology ; 32(5): 573, 1982 May.

Artigo em Inglês | MEDLINE | ID: mdl-7200217

13.

Practical management of neuromuscular diseases in the elderly.

Ringel, S P; Simon, D B.

Geriatrics ; 38(6): 86-92, 1983 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-6852533

14.

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.

Simon, D B; Lifton, R P.

Am J Physiol ; 271(5 Pt 2): F961-6, 1996 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-8945989

15.

Ion transporter mutations in Gitelman's and Bartter's syndromes.

Simon, D B; Lifton, R P.

Curr Opin Nephrol Hypertens ; 7(1): 43-7, 1998 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-9442362

16.

Neuropsychological findings in myotonic dystrophy.

Woodward, J B; Heaton, R K; Simon, D B; Ringel, S P.

J Clin Neuropsychol ; 4(4): 335-42, 1982 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-7174839

17.

Strontium-87m lung scans in pulmonary aspergillosis.

Rohatgi, P K; Simon, D B; Goldstein, R A; Reba, R C.

AJR Am J Roentgenol ; 129(5): 879-82, 1977 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-410255

18.

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases.

Su, I H; Frank, R; Gauthier, B G; Valderrama, E; Simon, D B; Lifton, R P; Trachtman, H.

Pediatr Nephrol ; 14(10-11): 970-2, 2000 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-10975308

19.

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

Cruz, D N; Shaer, A J; Bia, M J; Lifton, R P; Simon, D B.

Kidney Int ; 59(2): 710-7, 2001 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-11168953

20.

Mutations in the Na-Cl cotransporter reduce blood pressure in humans.

Cruz, D N; Simon, D B; Nelson-Williams, C; Farhi, A; Finberg, K; Burleson, L; Gill, J R; Lifton, R P.

Hypertension ; 37(6): 1458-64, 2001 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-11408395

Biblioteca Virtual em Saúde

Saúde Pública Brasil

Sua seleção (0)

Formato de exportação:

Exportar:

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Human hypertension caused by mutations in WNK kinases.

The role of Cas8 in type I CRISPR interference.

Symptomatic osseous sarcoidosis with findings on bone scan.

Unusual causes of stroke in a young adult.

Luetic meningitis with gumma.

Practical management of neuromuscular diseases in the elderly.

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.

Ion transporter mutations in Gitelman's and Bartter's syndromes.

Neuropsychological findings in myotonic dystrophy.

Strontium-87m lung scans in pulmonary aspergillosis.

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases.

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

Mutations in the Na-Cl cotransporter reduce blood pressure in humans.