Lang S - Search Results

1

Utilization of Online Resources by Patients in an Ophthalmic Emergency Department.

Hwang JC, Yannuzzi NA, Cavuoto KM, Ansari Z, Patel NA, Goodman CF, Lang S, Sridhar J. Hwang JC, et al. Among authors: lang s. J Acad Ophthalmol (2017). 2021 Dec 11;13(2):e247-e255. doi: 10.1055/s-0040-1722310. eCollection 2021 Jul. J Acad Ophthalmol (2017). 2021. PMID: 37388833 Free PMC article.

2

The North American Registry for Care and Research in Multiple Sclerosis (NARCRMS).

Rammohan KW, Halper J, Lang S, Murphy SM, Patton L, Goodman C, Li DKB. Rammohan KW, et al. Among authors: lang s. Int J MS Care. 2021 Nov-Dec;23(6):269-275. doi: 10.7224/1537-2073.2021-021. Epub 2021 Dec 29. Int J MS Care. 2021. PMID: 35035298 Free PMC article.

3

Effects of Mitomycin-C and 5-Fluorouracil on Ocular Adnexal Sebaceous Carcinoma Cells.

Gallo RA, Lang SH, Gomez A, Sabater AL, Tse DT, Pelaez D, Rong AJ. Gallo RA, et al. Am J Ophthalmol. 2022 Aug;240:14-22. doi: 10.1016/j.ajo.2021.12.016. Epub 2022 Jan 4. Am J Ophthalmol. 2022. PMID: 34995523 Free PMC article.

4

A novel pathogenic variant at the C-terminal propeptide cleavage site of COL1A1, causing osteogenesis imperfecta with intrafamilial variability.

Lang SH, Gallo RA, Forghani I. Lang SH, et al. Am J Med Genet A. 2022 Jun;188(6):1885-1889. doi: 10.1002/ajmg.a.62712. Epub 2022 Mar 3. Am J Med Genet A. 2022. PMID: 35243755

5

Derivation and Characterization of Murine and Amphibian Müller Glia Cell Lines.

Gallo RA, Qureshi F, Strong TA, Lang SH, Pino KA, Dvoriantchikova G, Pelaez D. Gallo RA, et al. Transl Vis Sci Technol. 2022 Apr 1;11(4):4. doi: 10.1167/tvst.11.4.4. Transl Vis Sci Technol. 2022. PMID: 35377941 Free PMC article.

6

EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder.

Forghani I, Lang SH, Rodier MJ, Bivona SA; Undiagnosed Diseases Network; Morales AA, Zuchner S, Bademci G, Tekin M. Forghani I, et al. Among authors: lang sh. Am J Med Genet A. 2024 Jun;194(6):e63556. doi: 10.1002/ajmg.a.63556. Epub 2024 Feb 13. Am J Med Genet A. 2024. PMID: 38348595

7

Multiple Mitochondrial Dysfunction Syndrome Type 3: A Likely Pathogenic Homozygous Variant Affecting a Patient of Cuban Descent and Literature Review.

Lang SH, Camponeschi F, Joya E, Borjas-Mendoza P, Tekin M, Thorson W. Lang SH, et al. Genes (Basel). 2022 Nov 6;13(11):2044. doi: 10.3390/genes13112044. Genes (Basel). 2022. PMID: 36360281 Free PMC article. Review.

8

Spectroelectrochemistry and light active process at nanointerface: general discussion.

Ding Z, Ewing AG, Fu KX, Hill CM, Hiramoto K, Kanoufi F, Kasianowicz JJ, Kranz C, Kuttner C, Lang SY, Li F, Liu L, Lu J, Mount AR, Ren H, Shao Y, Shen M, Takahashi Y, Wang W, Xia F, Zhang G, Zhao Z, Zhou Y. Ding Z, et al. Among authors: lang sy. Faraday Discuss. 2025 Jan 27. doi: 10.1039/d4fd90070g. Online ahead of print. Faraday Discuss. 2025. PMID: 39866054 No abstract available.

9

Synthetic GPR84 Agonists in Colorectal Cancer: Effective in THP-1 Cells but Ineffective in BMDMs and MC38 Mouse Tumor Models.

Schwarzfischer M, Walker MR, Curcio M, Boshta NM, Marchand A, Soons E, Pöhlmann D, Wawrzyniak M, Morsy Y, Lang S, Spalinger MR, Versele M, Scharl M. Schwarzfischer M, et al. Among authors: lang s. Int J Mol Sci. 2025 Jan 9;26(2):490. doi: 10.3390/ijms26020490. Int J Mol Sci. 2025. PMID: 39859206 Free PMC article.

10

Neuroendoscopic lavage for posthemorrhagic hydrocephalus of prematurity: preliminary results at a single institution in the United States.

Flanders TM, Hwang M, Julian NW, Sarris CE, Flibotte JJ, DeMauro SB, Munson DA, Heimall LM, Collins YC, Bamberski JM, Sturak MA, Storm PB, Lang SS, Heuer GG. Flanders TM, et al. Among authors: lang ss. J Neurosurg Pediatr. 2025 Jan 24:1-8. doi: 10.3171/2024.10.PEDS24119. Online ahead of print. J Neurosurg Pediatr. 2025. PMID: 39854725

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