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Items: 10

1.

Therapeutic Insights in Melasma and Hyperpigmentation Management

Huerth KA, Hassan S, Callender VD.

J Drugs Dermatol. 2019 Aug 1;18(8):718-729.

PMID:
31424704
2.

Drug Induced Pigmentation.

Hassan S, Zhou X.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2019 Jan-.
2019 Jun 30.

3.

Ophthalmological findings in Gaucher disease.

Eghbali A, Hassan S, Seehra G, FitzGibbon E, Sidransky E.

Mol Genet Metab. 2019 May;127(1):23-27. doi: 10.1016/j.ymgme.2019.02.002. Epub 2019 Feb 15. Review.

PMID:
31047801
4.

Precision Preventive Medicine-Ready for Prime Time?

Greenland P, Hassan S.

JAMA Intern Med. 2019 May 1;179(5):605-606. doi: 10.1001/jamainternmed.2019.0142. No abstract available.

PMID:
30882848
5.

Trauma-associated Pott's puffy tumor: an ophthalmologic perspective.

Hassan S, Rahmani B, Rastatter JC, Jaju AI, Kurup SP.

Orbit. 2019 Feb 18:1-3. doi: 10.1080/01676830.2019.1573909. [Epub ahead of print]

PMID:
30773962
6.

Epithelial ingrowth through venting incision into laser-assisted in situ keratomileusis flap interface after descemet stripping automated endothelial keratoplasty.

Ciocco L, Hassan S, Woreta F, Srikumaran D.

Am J Ophthalmol Case Rep. 2018 Nov 14;13:25-27. doi: 10.1016/j.ajoc.2018.11.012. eCollection 2019 Mar.

7.

Exploring genetic modifiers of Gaucher disease: The next horizon.

Davidson BA, Hassan S, Garcia EJ, Tayebi N, Sidransky E.

Hum Mutat. 2018 Dec;39(12):1739-1751. doi: 10.1002/humu.23611. Epub 2018 Sep 11. Review.

PMID:
30098107
8.

Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher disease.

Hassan S, Lopez G, Stubblefield BK, Tayebi N, Sidransky E.

Mol Genet Metab. 2018 Sep;125(1-2):1-3. doi: 10.1016/j.ymgme.2018.06.013. Epub 2018 Jun 28.

9.

Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course.

Tayebi N, Parisiadou L, Berhe B, Gonzalez AN, Serra-Vinardell J, Tamargo RJ, Maniwang E, Sorrentino Z, Fujiwara H, Grey RJ, Hassan S, Blech-Hermoni YN, Chen C, McGlinchey R, Makariou-Pikis C, Brooks M, Ginns EI, Ory DS, Giasson BI, Sidransky E.

Mol Genet Metab. 2017 Dec;122(4):198-208. doi: 10.1016/j.ymgme.2017.11.001. Epub 2017 Nov 21.

10.

The role of epigenetics in lysosomal storage disorders: Uncharted territory.

Hassan S, Sidransky E, Tayebi N.

Mol Genet Metab. 2017 Nov;122(3):10-18. doi: 10.1016/j.ymgme.2017.07.012. Epub 2017 Aug 1. Review.

PMID:
28918065

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