McLendon L - Search Results

1

Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosis.

Zhong N, Wisniewski KE, Hartikainen J, Ju W, Moroziewicz DN, McLendon L, Sklower Brooks SS, Brown WT. Zhong N, et al. Among authors: mclendon l. Clin Genet. 1998 Sep;54(3):234-8. doi: 10.1111/j.1399-0004.1998.tb04291.x. Clin Genet. 1998. PMID: 9788728

2

Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene.

Zhong N, Wisniewski KE, Kaczmarski AL, Ju W, Xu WM, Xu WW, Mclendon L, Liu B, Kaczmarski W, Sklower Brooks SS, Brown WT. Zhong N, et al. Among authors: mclendon l. Hum Genet. 1998 Jan;102(1):57-62. doi: 10.1007/s004390050654. Hum Genet. 1998. PMID: 9490299

3

Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene.

Hartikainen JM, Ju W, Wisniewski KE, Moroziewicz DN, Kaczmarski AL, McLendon L, Zhong D, Suarez CT, Brown WT, Zhong N. Hartikainen JM, et al. Among authors: mclendon l. Mol Genet Metab. 1999 Jun;67(2):162-8. doi: 10.1006/mgme.1999.2853. Mol Genet Metab. 1999. PMID: 10356316

4

Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses.

Zhong NA, Wisniewski KE, Ju W, Moroziewicz DN, Jurkiewicz A, McLendon L, Jenkins EC, Brown WT. Zhong NA, et al. Among authors: mclendon l. Genet Test. 2000;4(3):243-8. doi: 10.1089/10906570050501452. Genet Test. 2000. PMID: 11142754

5

Chronic Recurrent Multifocal Osteomyelitis Involving the Spine, Sternum, and Lower Extremities: A Case Report.

Huynh K, McLendon L, Woolnough L, Elder ME. Huynh K, et al. Among authors: mclendon l. Pediatrics. 2024 Oct 1;154(4):e2024067527. doi: 10.1542/peds.2024-067527. Pediatrics. 2024. PMID: 39323407

6

Muscle degeneration in aging Drosophila flies: the role of mechanical stress.

Chechenova M, McLendon L, Dallas B, Stratton H, Kiani K, Gerberich E, Alekseyenko A, Tamba N, An S, Castillo L, Czajkowski E, Talley C, Brown A, Bryantsev AL. Chechenova M, et al. Among authors: mclendon l. Skelet Muscle. 2024 Aug 20;14(1):20. doi: 10.1186/s13395-024-00352-4. Skelet Muscle. 2024. PMID: 39164781 Free PMC article.

7

Invasive Multimodality Neuromonitoring to Manage Cerebral Edema in Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.

Fainberg NA, Silver MR, Arena JD, Landzberg EI, Banwell B, Gambrah-Lyles C, Kirschen MP, Madsen PJ, McLendon L, Narula S, Tucker AM, Huh JW, Kienzle MF. Fainberg NA, et al. Among authors: mclendon l. Crit Care Explor. 2023 Nov 2;5(11):e1003. doi: 10.1097/CCE.0000000000001003. eCollection 2023 Nov. Crit Care Explor. 2023. PMID: 37929184 Free PMC article.

8

Dramatic Response to Anti-IL-6 Receptor Therapy in Children With Life-Threatening Myelin Oligodendrocyte Glycoprotein-Associated Disease.

McLendon LA, Gambrah-Lyles C, Viaene A, Fainberg NA, Landzberg EI, Tucker AM, Madsen PJ, Huh J, Silver MR, Arena JD, Kienzle MF, Banwell B. McLendon LA, et al. Neurol Neuroimmunol Neuroinflamm. 2023 Aug 15;10(6):e200150. doi: 10.1212/NXI.0000000000200150. Print 2023 Nov. Neurol Neuroimmunol Neuroinflamm. 2023. PMID: 37582615 Free PMC article.

9

HPV Vaccination among College Students in the South: The Role of HPV Knowledge on Vaccine Initiation and Completion.

Lee HY, Daniel CL, Wang K, McLendon L, Coyne-Beasley T. Lee HY, et al. Among authors: mclendon l. Asian Pac J Cancer Prev. 2023 Jun 1;24(6):2149-2156. doi: 10.31557/APJCP.2023.24.6.2149. Asian Pac J Cancer Prev. 2023. PMID: 37378947 Free PMC article.

10

A three-year-old with central nervous system graft versus host disease: A rare cause of posthematopoietic stem cell transplant encephalopathy.

Agrawal P, Nordli DR 3rd, McLendon LA. Agrawal P, et al. Among authors: mclendon la. Pediatr Blood Cancer. 2023 Aug;70(8):e30307. doi: 10.1002/pbc.30307. Epub 2023 May 12. Pediatr Blood Cancer. 2023. PMID: 37170842 No abstract available.

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