PubMed

Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes.

Rubio-Cabezas O, Edghill EL, Argente J, Hattersley AT.

Diabet Med. 2009 Oct;26(10):1070-4.PMID: 19900242 [PubMed - in process]Related articles

Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.

Rubio-Cabezas O, Patch AM, Minton JA, Flanagan SE, Edghill EL, Hussain K, Balafrej A, Deeb A, Buchanan CR, Jefferson IG, Mutair A; Neonatal Diabetes International Collaborative Group, Hattersley AT, Ellard S.

J Clin Endocrinol Metab. 2009 Nov;94(11):4162-70. Epub 2009 Oct 16.PMID: 19837917 [PubMed - in process]Related articlesFree article

Diagnosing monogenic diabetes: common misinterpretations of genetic findings.

Rubio-Cabezas O.

Pediatr Diabetes. 2009 Aug 31. [Epub ahead of print] No abstract available. PMID: 19732375 [PubMed - as supplied by publisher]Related articles

Mutations in the SLC29A3 gene are not a common cause of isolated autoantibody negative type 1 diabetes.

Edghill EL, Hameed S, Verge CF, Rubio-Cabezas O, Argente J, Sumnik Z, Dusatkova P, Cliffe ST, Hennekam RC, Buckley MF, Hussain K, Ellard S, Attersley AT.

JOP. 2009 Jul 6;10(4):457-8. No abstract available. PMID: 19581757 [PubMed - indexed for MEDLINE]Related articlesFree article

Tooth discoloration in patients with neonatal diabetes after transfer onto glibenclamide: a previously unreported side effect.

Kumaraguru J, Flanagan SE, Greeley SA, Nuboer R, Støy J, Philipson LH, Hattersley AT, Rubio-Cabezas O.

Diabetes Care. 2009 Aug;32(8):1428-30. Epub 2009 May 12.PMID: 19435956 [PubMed - indexed for MEDLINE]Related articlesFree article

A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients.

Shepherd M, Shields B, Ellard S, Rubio-Cabezas O, Hattersley AT.

Diabet Med. 2009 Apr;26(4):437-41.PMID: 19388975 [PubMed - indexed for MEDLINE]Related articles

Current insights into the genetic basis of diabetes mellitus in children and adolescents.

Rubio-Cabezas O, Argente J.

J Pediatr Endocrinol Metab. 2008 Oct;21(10):917-40. Review.PMID: 19209614 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.

Rubio-Cabezas O, Minton JA, Caswell R, Shield JP, Deiss D, Sumnik Z, Cayssials A, Herr M, Loew A, Lewis V, Ellard S, Hattersley AT.

Diabetes Care. 2009 Jan;32(1):111-6. Epub 2008 Oct 17.PMID: 18931102 [PubMed - in process]Related articlesFree article

Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene.

Rubio-Cabezas O, Díaz González F, Aragonés A, Argente J, Campos-Barros A.

Pediatr Diabetes. 2008 Jun;9(3 Pt 1):245-9. Epub 2008 Feb 21.PMID: 18298419 [PubMed - indexed for MEDLINE]Related articles

[Diabetes mellitus in children: a heterogeneous disease]

Rubio Cabezas O, Argente Oliver J.

Med Clin (Barc). 2007 Apr 28;128(16):627-33. Review. Spanish. PMID: 17524322 [PubMed - indexed for MEDLINE]Related articles

[Diabetes mellitus in children and adolescents: chronic complications and associated diseases]

Rubio Cabezas O, Argente Oliver J.

An Pediatr (Barc). 2007 Mar;66(3):282-9. Review. Spanish. PMID: 17349255 [PubMed - indexed for MEDLINE]Related articlesFree article

[Treatment with continuous subcutaneous insulin infusion in pediatric patients with type 1 diabetes mellitus]

Rubio Cabezas O, Argenté Oliver J.

An Pediatr (Barc). 2006 Jun;64(6):600-1; author reply 601-2. Spanish. No abstract available. PMID: 16792974 [PubMed - indexed for MEDLINE]Related articlesFree article

[Hyperinsulinism-hyperammonemia syndrome due to a de novo mutation in exon 7 (G979A) of the glutamate dehydrogenase gene with excellent response to diazoxide]

Montero Luis C, Pozo Román J, Muñoz Calvo MT, Martos Moreno G, Donoso MA, Rubio Cabezas O, Argente Oliver J.

An Pediatr (Barc). 2004 Nov;61(5):433-7. Spanish. PMID: 15530324 [PubMed - indexed for MEDLINE]Related articlesFree article

[Graves' disease in children: management and review of 20 patients]

Rubio Cabezas O, Muñoz Calvo MT, Pozo Román J, Argente Oliver J.

An Pediatr (Barc). 2004 Aug;61(2):131-6. Spanish. PMID: 15274877 [PubMed - indexed for MEDLINE]Related articlesFree article