Found: 5
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A case of early-onset familial Alzheimer’s disease with both APP and novel PSEN2 mutations presenting with non-amnestic features.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Guidelines on retention of pathology records and materials (Version 2/2022).
- Published in:
- Malaysian Journal of Pathology, 2022, v. 44, n. 2, p. 165
- By:
- Publication type:
- Article
Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism.
- Published in:
- Arthritis & Rheumatology, 2016, v. 68, n. 4, p. 1039, doi. 10.1002/art.39519
- By:
- Publication type:
- Article
Outcomes of Patients with EGFR-Mutant Advanced NSCLC in a Developing Country in Southeast Asia.
- Published in:
- Cancer Management & Research, 2022, v. 14, p. 1995, doi. 10.2147/CMAR.S364713
- By:
- Publication type:
- Article