Found: 7
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Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation.
- Published in:
- 2017
- By:
- Publication type:
- case study
Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 216, doi. 10.1002/pd.2440
- By:
- Publication type:
- Article
Bilateral fetal hyperechogenic kidneys associated with normal amniotic fluid: an ethical dilemma in a normal variant?
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 190, doi. 10.1002/pd.1377
- By:
- Publication type:
- Article
Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 6, p. 777, doi. 10.1002/acn3.568
- By:
- Publication type:
- Article
Chemical composition of the oil and supercritical CO<sub>2</sub> extract of Schinus molle L.
- Published in:
- Flavour & Fragrance Journal, 2004, v. 19, n. 6, p. 554, doi. 10.1002/ffj.1350
- By:
- Publication type:
- Article
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
- Published in:
- Journal of Neurology, 2017, v. 264, n. 7, p. 1426, doi. 10.1007/s00415-017-8540-x
- By:
- Publication type:
- Article
A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 10, p. 2373, doi. 10.1007/s00415-015-7896-z
- By:
- Publication type:
- Article