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Results: 1 to 20 of 23

1.

Effect of pioglitazone on the course of new-onset type 1 diabetes mellitus.

Tafuri KS, Godil MA, Lane AH, Wilson TA.

J Clin Res Pediatr Endocrinol. 2013;5(4):236-9. doi: 10.4274/Jcrpe.981.

2.

Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.

Lekarev O, Tafuri K, Lane AH, Zhu G, Nakamoto JM, Buller-Burckle AM, Wilson TA, New MI.

J Perinatol. 2013 Jan;33(1):76-8. doi: 10.1038/jp.2012.5.

PMID:
23269230
3.

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

Snape K, Hanks S, Ruark E, Barros-Núñez P, Elliott A, Murray A, Lane AH, Shannon N, Callier P, Chitayat D, Clayton-Smith J, Fitzpatrick DR, Gisselsson D, Jacquemont S, Asakura-Hay K, Micale MA, Tolmie J, Turnpenny PD, Wright M, Douglas J, Rahman N.

Nat Genet. 2011 Jun;43(6):527-9. doi: 10.1038/ng.822. Epub 2011 May 8.

4.

The effect of oral leucine on protein metabolism in adolescents with type 1 diabetes mellitus.

Desikan V, Mileva I, Garlick J, Lane AH, Wilson TA, McNurlan MA.

Int J Pediatr Endocrinol. 2010;2010:493258. doi: 10.1155/2010/493258. Epub 2010 Dec 19.

5.

Effect of inspiration/expiration on height measurement.

Kacer M, Zhang G, Lane AH, Chen JJ, Wilson TA.

J Pediatr Endocrinol Metab. 2008 Aug;21(8):763-9.

PMID:
18825876
6.
7.

Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus.

Tegay DH, Lane AH, Roohi J, Hatchwell E.

Am J Med Genet A. 2007 Mar 15;143A(6):594-8.

PMID:
17318848
8.

Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.

Leipoldt M, Erdel M, Bien-Willner GA, Smyk M, Theurl M, Yatsenko SA, Lupski JR, Lane AH, Shanske AL, Stankiewicz P, Scherer G.

Clin Genet. 2007 Jan;71(1):67-75.

PMID:
17204049
9.

Use of subcutaneous DDAVP in infants with central diabetes insipidus.

Blanco EJ, Lane AH, Aijaz N, Blumberg D, Wilson TA.

J Pediatr Endocrinol Metab. 2006 Jul;19(7):919-25.

PMID:
16995572
10.

Neurocognitive function in children with compensated hypothyroidism: lack of short term effects on or off thyroxin.

Aijaz NJ, Flaherty EM, Preston T, Bracken SS, Lane AH, Wilson TA.

BMC Endocr Disord. 2006 Mar 20;6:2.

11.

Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A.

Lane AH, Markarian K, Braziunene I.

J Pediatr Endocrinol Metab. 2004 Dec;17(12):1679-82.

PMID:
15645704
12.

Type 1 diabetes mellitus masked by primary adrenal insufficiency in a child with autoimmune polyglandular syndrome type 2.

Aijaz NJ, Blanco E, Lane AH, Wilson TA.

Clin Pediatr (Phila). 2003 Jan-Feb;42(1):75-7. No abstract available.

PMID:
12635986
13.

Mosaic variegated aneuploidy with growth hormone deficiency and congenital heart defects.

Lane AH, Aijaz N, Galvin-Parton P, Lanman J, Mangano R, Wilson TA.

Am J Med Genet. 2002 Jul 1;110(3):273-7.

PMID:
12116237
14.
15.

Congenital nasal pyriform aperture stenosis associated with central diabetes insipidus.

Godil MA, Galvin-Parton P, Monte D, Zerah M, Purandare A, Lane AH, Wilson TA.

J Pediatr. 2000 Aug;137(2):260-2.

PMID:
10931423
16.
17.

Diagnostic utility of Müllerian inhibiting substance determination in patients with primary and recurrent granulosa cell tumors.

Lane AH, Lee MM, Fuller AF Jr, Kehas DJ, Donahoe PK, MacLaughlin DT.

Gynecol Oncol. 1999 Apr;73(1):51-5.

PMID:
10094880
18.

New insights into mullerian inhibiting substance and its mechanism of action.

Lane AH, Donahoe PK.

J Endocrinol. 1998 Jul;158(1):1-6. Review.

19.

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.

Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Farmer GE, Lamiell JM, Haines J, Yuen JW, Collins D, Majoor-Krakauer D, et al.

Nature. 1988 Mar 17;332(6161):268-9.

PMID:
2894613
20.

Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.

Seizinger BR, Rouleau GA, Lane AH, Farmer G, Ozelius LJ, Haines JL, Parry DM, Korf BR, Pericak-Vance MA, Faryniarz AG, et al.

Genomics. 1987 Dec;1(4):346-8.

PMID:
2896628
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