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Steven S Chin

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The American Journal of Pathology|November 30, 2005

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJDManuela Pastore, Steven S Chin, Karen L Bell, et al.

Neurosurgery|October 22, 2005

Clinicopathological review: giant cell reparative granuloma of the orbitAnthony L D'Ambrosio, Susan C Williams, Angela Lignelli, et al.

The Journal of Clinical Investigation|February 16, 2008

Proteomic identification of FHL1 as the protein mutated in human reducing body myopathyJoachim Schessl, Yaqun Zou, Meagan J McGrath, et al.

Brain : a Journal of Neurology|February 3, 2009

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1Joachim Schessl, Ana L Taratuto, Caroline Sewry, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 34 results.

The American Journal of Pathology|November 30, 2005

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJDManuela Pastore, Steven S Chin, Karen L Bell, et al.

Neurosurgery|October 22, 2005

Clinicopathological review: giant cell reparative granuloma of the orbitAnthony L D'Ambrosio, Susan C Williams, Angela Lignelli, et al.

The Journal of Clinical Investigation|February 16, 2008

Proteomic identification of FHL1 as the protein mutated in human reducing body myopathyJoachim Schessl, Yaqun Zou, Meagan J McGrath, et al.

Brain : a Journal of Neurology|February 3, 2009

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1Joachim Schessl, Ana L Taratuto, Caroline Sewry, et al.

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