Babovic-Vuksanovic D - Search Results

1

Bilateral pheochromocytomas in a child who had hemihypertrophy and alteration in the VHL gene.

Amini Z, Babovic-Vuksanovic D, Lteif A. Amini Z, et al. J Pediatr Endocrinol Metab. 2013;26(3-4):369-72. doi: 10.1515/jpem-2012-0255. J Pediatr Endocrinol Metab. 2013. PMID: 23327821

2

Mayer-Rokitansky-Küster-Hauser anomaly and its associated malformations.

Pittock ST, Babovic-Vuksanovic D, Lteif A. Pittock ST, et al. Am J Med Genet A. 2005 Jun 15;135(3):314-6. doi: 10.1002/ajmg.a.30721. Am J Med Genet A. 2005. PMID: 15887261

3

Vitamin A deficiency in an infant with PAGOD syndrome.

Gavrilova R, Babovic N, Lteif A, Eidem B, Kirmani S, Olson T, Babovic-Vuksanovic D. Gavrilova R, et al. Am J Med Genet A. 2009 Oct;149A(10):2241-7. doi: 10.1002/ajmg.a.32998. Am J Med Genet A. 2009. PMID: 19760653

4

Bilateral pheochromocytoma: Clinical characteristics, treatment and longitudinal follow-up.

Kittah NE, Gruber LM, Bancos I, Hamidi O, Tamhane S, Iñiguez-Ariza N, Babovic-Vuksanovic D, Thompson GB, Lteif A, Young WF, Erickson D. Kittah NE, et al. Clin Endocrinol (Oxf). 2020 Sep;93(3):288-295. doi: 10.1111/cen.14222. Epub 2020 Jun 22. Clin Endocrinol (Oxf). 2020. PMID: 32410303

5

Pheochromocytoma and paraganglioma in patients with neurofibromatosis type 1.

Gruber LM, Erickson D, Babovic-Vuksanovic D, Thompson GB, Young WF Jr, Bancos I. Gruber LM, et al. Clin Endocrinol (Oxf). 2017 Jan;86(1):141-149. doi: 10.1111/cen.13163. Epub 2016 Aug 26. Clin Endocrinol (Oxf). 2017. PMID: 27460956

6

When Biochemical Phenotype Predicts Genotype: Pheochromocytoma and Paraganglioma.

Yan Q, Bancos I, Gruber LM, Bancos C, McKenzie TJ, Babovic-Vuksanovic D, Young WF Jr. Yan Q, et al. Am J Med. 2018 May;131(5):506-509. doi: 10.1016/j.amjmed.2018.01.010. Epub 2018 Jan 31. Am J Med. 2018. PMID: 29391129 No abstract available.

7

Extensive acrochordons and pancreatic islet-cell tumors in tuberous sclerosis associated with TSC2 mutations.

Merritt JL 2nd, Davis DM, Pittelkow MR, Babovic-Vuksanovic D. Merritt JL 2nd, et al. Am J Med Genet A. 2006 Aug 1;140(15):1669-72. doi: 10.1002/ajmg.a.31351. Am J Med Genet A. 2006. PMID: 16835931

8

Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.

Dhamija R, Kirmani S, Wang X, Ferber MJ, Wieben ED, Lazaridis KN, Babovic-Vuksanovic D. Dhamija R, et al. Am J Med Genet A. 2014 Sep;164A(9):2356-9. doi: 10.1002/ajmg.a.36621. Epub 2014 May 28. Am J Med Genet A. 2014. PMID: 24888332

9

Management and outcome of neonatal-onset ornithine transcarbamylase deficiency following liver transplantation at 60 days of life.

Ensenauer R, Tuchman M, El-Youssef M, Kotagal S, Ishitani MB, Matern D, Babovic-Vuksanovic D. Ensenauer R, et al. Mol Genet Metab. 2005 Apr;84(4):363-6. doi: 10.1016/j.ymgme.2004.12.011. Mol Genet Metab. 2005. PMID: 15781198

10

A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma.

Kitzmann AS, Pulido JS, Ferber MJ, Highsmith WE, Babovic-Vuksanovic D. Kitzmann AS, et al. Ophthalmic Genet. 2006 Dec;27(4):157-9. doi: 10.1080/13816810600977168. Ophthalmic Genet. 2006. PMID: 17148043

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

141 results

Search Page

Filters