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Items: 6

1.

Variation in cognitive function over time in Gaucher disease type 3.

Steward AM, Wiggs E, Lindstrom T, Ukwuani S, Ryan E, Tayebi N, Roshan Lal T, Lopez G, Schiffmann R, Sidransky E.

Neurology. 2019 Nov 12. pii: 10.1212/WNL.0000000000008618. doi: 10.1212/WNL.0000000000008618. [Epub ahead of print]

PMID:
31719137
2.

Five-parameter evaluation of dysphagia: A novel prognostic scale for assessing neurological decline in Gaucher disease type 2.

Seehra G, Solomon B, Ryan E, Steward AM, Roshan Lal T, Tanima Y, Lopez G, Sidransky E.

Mol Genet Metab. 2019 Jul;127(3):191-199. doi: 10.1016/j.ymgme.2019.06.002. Epub 2019 Jun 8.

PMID:
31256856
3.

Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase gene.

Hagege E, Grey RJ, Lopez G, Roshan Lal T, Sidransky E, Tayebi N.

Am J Med Genet A. 2017 Dec;173(12):3211-3215. doi: 10.1002/ajmg.a.38487. Epub 2017 Nov 1.

4.

The Spectrum of Neurological Manifestations Associated with Gaucher Disease.

Roshan Lal T, Sidransky E.

Diseases. 2017 Mar 2;5(1). pii: E10. doi: 10.3390/diseases5010010. Review.

5.

Induced pluripotent stem cell models of lysosomal storage disorders.

Borger DK, McMahon B, Roshan Lal T, Serra-Vinardell J, Aflaki E, Sidransky E.

Dis Model Mech. 2017 Jun 1;10(6):691-704. doi: 10.1242/dmm.029009. Review.

6.

Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.

Roshan Lal TR, Kliewer MA, Lopes T, Rebsamen SL, O'Connor J, Grados MA, Kimball A, Clemens J, Kline AD.

Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):190-7. doi: 10.1002/ajmg.c.31503. Epub 2016 May 10.

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