Leonard JV - Search Results

1

Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1.

Visser G, Rake JP, Labrune P, Leonard JV, Moses S, Ullrich K, Wendel U, Groenier KH, Smit GP. Visser G, et al. Among authors: leonard jv. Eur J Pediatr. 2002 Oct;161 Suppl 1:S83-7. doi: 10.1007/s00431-002-1010-0. Epub 2002 Jul 17. Eur J Pediatr. 2002. PMID: 12373578

2

Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I).

Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GP. Rake JP, et al. Among authors: leonard jv. Eur J Pediatr. 2002 Oct;161 Suppl 1:S20-34. doi: 10.1007/s00431-002-0999-4. Epub 2002 Aug 22. Eur J Pediatr. 2002. PMID: 12373567

3

Guidelines for management of glycogen storage disease type I - European Study on Glycogen Storage Disease Type I (ESGSD I).

Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GP; European Study on Glycogen Storage Disease Type I (ESGSD I). Rake JP, et al. Among authors: leonard jv. Eur J Pediatr. 2002 Oct;161 Suppl 1:S112-9. doi: 10.1007/s00431-002-1016-7. Epub 2002 Aug 24. Eur J Pediatr. 2002. PMID: 12373584 Review.

4

Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1.

Visser G, Rake JP, Labrune P, Leonard JV, Moses S, Ullrich K, Wendel U, Smit GP; European Study on Glycogen Storage Disease Type I. Visser G, et al. Among authors: leonard jv. Eur J Pediatr. 2002 Oct;161 Suppl 1:S120-3. doi: 10.1007/s00431-002-1017-6. Epub 2002 Sep 13. Eur J Pediatr. 2002. PMID: 12373585 Review.

5

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.

Santer R, Groth S, Kinner M, Dombrowski A, Berry GT, Brodehl J, Leonard JV, Moses S, Norgren S, Skovby F, Schneppenheim R, Steinmann B, Schaub J. Santer R, et al. Among authors: leonard jv. Hum Genet. 2002 Jan;110(1):21-9. doi: 10.1007/s00439-001-0638-6. Epub 2001 Nov 17. Hum Genet. 2002. PMID: 11810292

6

Utilization of cornstarch in glycogen storage disease type Ia.

Bodamer OA, Feillet F, Lane RE, Lee PJ, Dixon MA, Halliday D, Leonard JV. Bodamer OA, et al. Among authors: leonard jv. Eur J Gastroenterol Hepatol. 2002 Nov;14(11):1251-6. doi: 10.1097/00042737-200211000-00014. Eur J Gastroenterol Hepatol. 2002. PMID: 12439121

7

The regulation of growth in glycogen storage disease type 1.

Mundy HR, Hindmarsh PC, Matthews DR, Leonard JV, Lee PJ. Mundy HR, et al. Among authors: leonard jv. Clin Endocrinol (Oxf). 2003 Mar;58(3):332-9. doi: 10.1046/j.1365-2265.2003.01717.x. Clin Endocrinol (Oxf). 2003. PMID: 12608939

8

Hepatic ultrasound findings in the glycogen storage diseases.

Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C. Lee P, et al. Br J Radiol. 1994 Nov;67(803):1062-6. doi: 10.1259/0007-1285-67-803-1062. Br J Radiol. 1994. PMID: 7820397

9

Textbook on endocrinology.

Lee P, Leonard J. Lee P, et al. BMJ. 1994 Jun 4;308(6942):1512. doi: 10.1136/bmj.308.6942.1512c. BMJ. 1994. PMID: 8019301 Free PMC article. No abstract available.

10

Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease.

Broomfield A, Sweeney MG, Woodward CE, Fratter C, Morris AM, Leonard JV, Abulhoul L, Grunewald S, Clayton PT, Hanna MG, Poulton J, Rahman S. Broomfield A, et al. Among authors: leonard jv. J Inherit Metab Dis. 2015 May;38(3):445-57. doi: 10.1007/s10545-014-9778-4. Epub 2014 Oct 29. J Inherit Metab Dis. 2015. PMID: 25352051 Free PMC article.

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