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A Patient with Sjogren's Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis. [electronic resource] by
- Hom, Jason
- Marwaha, Shruti
- Postolova, Anna
- Kittle, Jessie
- Vasquez, Rosaline
- Davidson, Jean
- Kohler, Jennefer
- Dries, Annika
- Fernandez-Betancourt, Liliana
- Majcherska, Marta
- Dearlove, Joanna
- Raghavan, Shyam
- Vogel, Hannes
- Bernstein, Jonathan A
- Fisher, Paul
- Ashley, Euan
- Sampson, Jacinda
- Wheeler, Matthew
Producer: 20201008
In:
Journal of general internal medicine vol. 34
Availability: No items available.
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163.
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Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy. [electronic resource] by
- Broccolini, Aldobrando
- Ricci, Enzo
- Cassandrini, Denise
- Gliubizzi, Carla
- Bruno, Claudio
- Tonoli, Emmanuel
- Silvestri, Gabriella
- Pescatori, Mario
- Rodolico, Carmelo
- Sinicropi, Stefano
- Servidei, Serenella
- Zara, Federico
- Minetti, Carlo
- Tonali, Pietro A
- Mirabella, Massimiliano
Producer: 20040924
In:
Human mutation vol. 23
Availability: No items available.
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