Polak M - Search Results

1

ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents.

Greeley SAW, Polak M, Njølstad PR, Barbetti F, Williams R, Castano L, Raile K, Chi DV, Habeb A, Hattersley AT, Codner E. Greeley SAW, et al. Among authors: polak m. Pediatr Diabetes. 2022 Dec;23(8):1188-1211. doi: 10.1111/pedi.13426. Pediatr Diabetes. 2022. PMID: 36537518 Free PMC article. No abstract available.

2

Demonstration of lactogenic receptors in rat endocrine pancreases by quantitative autoradiography.

Polak M, Scharfmann R, Ban E, Haour F, Postel-Vinay MC, Czernichow P. Polak M, et al. Diabetes. 1990 Sep;39(9):1045-9. doi: 10.2337/diab.39.9.1045. Diabetes. 1990. PMID: 2166698

3

Case report: insulin-dependent diabetes mellitus in childhood associated with scleroderma.

Polak M, Le Luyer B, Rybojab M, Czernichow P. Polak M, et al. Diabetes Metab. 1996 Jun;22(3):192-6. Diabetes Metab. 1996. PMID: 8697307

4

Emergence of type 2 diabetes in an hospital based cohort of children with diabetes mellitus.

Ortega-Rodriguez E, Levy-Marchal C, Tubiana N, Czernichow P, Polak M. Ortega-Rodriguez E, et al. Among authors: polak m. Diabetes Metab. 2001 Nov;27(5 Pt 1):574-8. Diabetes Metab. 2001. PMID: 11694856

5

Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes.

Gloyn AL, Ellard S, Shield JP, Temple IK, Mackay DJ, Polak M, Barrett T, Hattersley AT. Gloyn AL, et al. Among authors: polak m. Diabetologia. 2002 Feb;45(2):290. doi: 10.1007/s00125-001-0746-9. Diabetologia. 2002. PMID: 11942315 No abstract available.

6

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

Vaxillaire M, Populaire C, Busiah K, Cavé H, Gloyn AL, Hattersley AT, Czernichow P, Froguel P, Polak M. Vaxillaire M, et al. Among authors: polak m. Diabetes. 2004 Oct;53(10):2719-22. doi: 10.2337/diabetes.53.10.2719. Diabetes. 2004. PMID: 15448107

7

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

Pearson ER, Flechtner I, Njølstad PR, Malecki MT, Flanagan SE, Larkin B, Ashcroft FM, Klimes I, Codner E, Iotova V, Slingerland AS, Shield J, Robert JJ, Holst JJ, Clark PM, Ellard S, Søvik O, Polak M, Hattersley AT; Neonatal Diabetes International Collaborative Group. Pearson ER, et al. Among authors: polak m. N Engl J Med. 2006 Aug 3;355(5):467-77. doi: 10.1056/NEJMoa061759. N Engl J Med. 2006. PMID: 16885550 Free article.

8

New ABCC8 mutations in relapsing neonatal diabetes and clinical features.

Vaxillaire M, Dechaume A, Busiah K, Cavé H, Pereira S, Scharfmann R, de Nanclares GP, Castano L, Froguel P, Polak M; SUR1-Neonatal Diabetes Study Group. Vaxillaire M, et al. Among authors: polak m. Diabetes. 2007 Jun;56(6):1737-41. doi: 10.2337/db06-1540. Epub 2007 Mar 27. Diabetes. 2007. PMID: 17389331

9

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.

Polak M, Dechaume A, Cavé H, Nimri R, Crosnier H, Sulmont V, de Kerdanet M, Scharfmann R, Lebenthal Y, Froguel P, Vaxillaire M; French ND (Neonatal Diabetes) Study Group. Polak M, et al. Diabetes. 2008 Apr;57(4):1115-9. doi: 10.2337/db07-1358. Epub 2008 Jan 2. Diabetes. 2008. PMID: 18171712

10

Neonatal diabetes mellitus because of pancreatic agenesis with dysmorphic features and recurrent bacterial infections.

Taha D, Bardise J, Hegab A, Bonnefond A, Marchand M, Drunat S, Vaxillaire M, Polak M. Taha D, et al. Among authors: polak m. Pediatr Diabetes. 2008 Jun;9(3 Pt 1):240-4. doi: 10.1111/j.1399-5448.2007.00365.x. Pediatr Diabetes. 2008. PMID: 18547237

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