Bartholomew D - Search Results

1

Docosahexaenoic Acid and Amino Acid Contents in Pasteurized Donor Milk are Low for Preterm Infants.

Valentine CJ, Morrow G, Fernandez S, Gulati P, Bartholomew D, Long D, Welty SE, Morrow AL, Rogers LK. Valentine CJ, et al. Among authors: bartholomew d. J Pediatr. 2010 Dec;157(6):906-10. doi: 10.1016/j.jpeds.2010.06.017. Epub 2010 Sep 17. J Pediatr. 2010. PMID: 20850762

2

Vitamin B12 deficiency associated with low breast-milk vitamin B12 concentration in an infant following maternal gastric bypass surgery.

Wardinsky TD, Montes RG, Friederich RL, Broadhurst RB, Sinnhuber V, Bartholomew D. Wardinsky TD, et al. Among authors: bartholomew d. Arch Pediatr Adolesc Med. 1995 Nov;149(11):1281-4. doi: 10.1001/archpedi.1995.02170240099020. Arch Pediatr Adolesc Med. 1995. PMID: 7581767 No abstract available.

3

Mehyar LS, Abu-Arja R, Rangarajan HG, Pai V, Bartholomew DW, Rose MJ, Bajwa RPS. Mehyar LS, et al. Bone Marrow Transplant. 2018 Aug;53(8):1076-1078. doi: 10.1038/s41409-018-0147-z. Epub 2018 Mar 7. Bone Marrow Transplant. 2018. PMID: 29515247 No abstract available.

4

Cranial nerve and cervical root enhancement in an infant with polymerase gamma mutation mitochondrial disease.

Horst DM, Ruess L, Rusin JA, Bartholomew DW. Horst DM, et al. Pediatr Neurol. 2014 Nov;51(5):734-6. doi: 10.1016/j.pediatrneurol.2014.06.015. Epub 2014 Jun 26. Pediatr Neurol. 2014. PMID: 25286830

5

Potential and pitfalls of NBS, and the reference lab's role.

Bartholomew DW. Bartholomew DW. MLO Med Lab Obs. 2007 Jul;39(7):12, 14-6, 19; quiz 26-7. MLO Med Lab Obs. 2007. PMID: 17695966 No abstract available.

6

m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening.

Mori M, Mytinger JR, Martin LC, Bartholomew D, Hickey S. Mori M, et al. Among authors: bartholomew d. JIMD Rep. 2014;17:47-51. doi: 10.1007/8904_2014_332. Epub 2014 Sep 21. JIMD Rep. 2014. PMID: 25240982 Free PMC article.

7

High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.

Tsao CY, Mendell JR, Bartholomew D. Tsao CY, et al. Among authors: bartholomew d. J Child Neurol. 2001 Jul;16(7):533-5. doi: 10.1177/088307380101600716. J Child Neurol. 2001. PMID: 11453454

8

Characterization of the renal phenotype in RMND1-related mitochondrial disease.

Shayota BJ, Le NT, Bekheirnia N, Rosenfeld JA, Goldstein AC, Moritz M, Bartholomew DW, Pastore MT, Xia F, Eng C, Yang Y, Lamb DJ, Scaglia F, Braun MC, Bekheirnia MR. Shayota BJ, et al. Mol Genet Genomic Med. 2019 Dec;7(12):e973. doi: 10.1002/mgg3.973. Epub 2019 Sep 30. Mol Genet Genomic Med. 2019. PMID: 31568715 Free PMC article.

9

Recurrent pancreatitis in ornithine transcarbamylase deficiency.

Prada CE, Kaul A, Hopkin RJ, Page KI, Nathan JD, Bartholomew DW, Cohen MB, Heubi JE, Leslie ND, Burrow TA. Prada CE, et al. Among authors: bartholomew dw. Mol Genet Metab. 2012 Aug;106(4):482-4. doi: 10.1016/j.ymgme.2012.06.005. Epub 2012 Jun 15. Mol Genet Metab. 2012. PMID: 22728053

10

Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant.

Arredondo K, Myers C, Hansen-Kiss E, Mathew MT, Jayaraman V, Siemon A, Bartholomew D, Herman GE, Mori M. Arredondo K, et al. Among authors: bartholomew d. J Child Neurol. 2022 May;37(6):517-523. doi: 10.1177/08830738221089741. Epub 2022 Apr 6. J Child Neurol. 2022. PMID: 35384780

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