Clark LN - Search Results

1

Grover disease (transient acantholytic dermatosis) in acute myeloid leukemia on FDG PET/CT.

Zhu HJ, Clark LN, Deloney LA, McDonald JE. Zhu HJ, et al. Among authors: clark ln. Clin Nucl Med. 2014 Feb;39(2):e173-5. doi: 10.1097/RLU.0000000000000252. Clin Nucl Med. 2014. PMID: 24152615

2

Neutropenic Enterocolitis: New Insights Into a Deadly Entity.

Sachak T, Arnold MA, Naini BV, Graham RP, Shah SS, Cruise M, Park JY, Clark L, Lamps L, Frankel WL, Theodoropoulos N, Arnold CA. Sachak T, et al. Am J Surg Pathol. 2015 Dec;39(12):1635-42. doi: 10.1097/PAS.0000000000000517. Am J Surg Pathol. 2015. PMID: 26414225

3

Nuclear factor XIIIa staining (clone AC-1A1 mouse monoclonal) is a sensitive and specific marker to discriminate sebaceous proliferations from other cutaneous clear cell neoplasms.

Uhlenhake EE, Clark LN, Smoller BR, Shalin SC, Gardner JM. Uhlenhake EE, et al. Among authors: clark ln. J Cutan Pathol. 2016 Aug;43(8):649-56. doi: 10.1111/cup.12726. Epub 2016 Jun 10. J Cutan Pathol. 2016. PMID: 27153339

4

Nuclear factor XIIIa staining (clone AC-1A1 mouse monoclonal) is a highly sensitive marker of sebaceous differentiation in normal and neoplastic sebocytes.

Clark LN, Elwood HR, Uhlenhake EE, Smoller BR, Shalin SC, Gardner JM. Clark LN, et al. J Cutan Pathol. 2016 Aug;43(8):657-62. doi: 10.1111/cup.12727. Epub 2016 Jun 14. J Cutan Pathol. 2016. PMID: 27153463

5

Idiopathic Hypereosinophilic Syndrome With Cutaneous Manifestations and Flame Figures: A Spectrum of Eosinophilic Dermatoses Whose Features Overlap With Wells' Syndrome.

Smith SM, Kiracofe EA, Clark LN, Gru AA. Smith SM, et al. Among authors: clark ln. Am J Dermatopathol. 2015 Dec;37(12):910-4. doi: 10.1097/DAD.0000000000000279. Am J Dermatopathol. 2015. PMID: 25839890 Free PMC article.

6

A phase I study to evaluate the safety, pharmacokinetics, and pharmacodynamics of PF-06939999 (PRMT5 inhibitor) in patients with selected advanced or metastatic tumors with high incidence of splicing factor gene mutations.

Rodon J, Rodriguez E, Maitland ML, Tsai FY, Socinski MA, Berlin JD, Thomas JS, Al Baghdadi T, Wang IM, Guo C, Golmakani M, Clark LN, Gazdoiu M, Li M, Tolcher AW. Rodon J, et al. Among authors: clark ln. ESMO Open. 2024 Apr;9(4):102961. doi: 10.1016/j.esmoop.2024.102961. Epub 2024 Apr 18. ESMO Open. 2024. PMID: 38640748 Free PMC article. Clinical Trial.

7

Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.

Clark LN, Gao Y, Wang GT, Hernandez N, Ashley-Koch A, Jankovic J, Ottman R, Leal SM, Rodriguez SMB, Louis ED. Clark LN, et al. EBioMedicine. 2022 Nov;85:104290. doi: 10.1016/j.ebiom.2022.104290. Epub 2022 Sep 29. EBioMedicine. 2022. PMID: 36183486 Free PMC article.

8

Lack of Familial Aggregation of the "Essential Tremor-Plus" Phenotype in Familial Essential Tremor.

Berry DS, Hernandez N, Clark LN, Louis ED. Berry DS, et al. Among authors: clark ln. Neuroepidemiology. 2022;56(5):373-379. doi: 10.1159/000526278. Epub 2022 Aug 8. Neuroepidemiology. 2022. PMID: 35940165 Free PMC article.

9

Clinical exome sequencing for inherited retinal degenerations at a tertiary care center.

Ganapathi M, Thomas-Wilson A, Buchovecky C, Dharmadhikari A, Barua S, Lee W, Ruan MZC, Soucy M, Ragi S, Tanaka J, Clark LN, Naini AB, Liao J, Mansukhani M, Tsang S, Jobanputra V. Ganapathi M, et al. Among authors: clark ln. Sci Rep. 2022 Jun 7;12(1):9358. doi: 10.1038/s41598-022-13026-2. Sci Rep. 2022. PMID: 35672425 Free PMC article.

10

Mixed Motor Disorder: Essential Tremor Families With Heterogeneous Motor Phenomenology.

Louis ED, Hernandez NC, Ottman R, Clark LN. Louis ED, et al. Among authors: clark ln. Neurol Clin Pract. 2021 Dec;11(6):e817-e825. doi: 10.1212/CPJ.0000000000001100. Neurol Clin Pract. 2021. PMID: 34992964 Free PMC article.

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