Found: 6
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Growth Hormone Deficiency due to p.(Gln467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome.
- Published in:
- Molecular Syndromology, 2022, v. 13, n. 5, p. 425, doi. 10.1159/000522532
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- Publication type:
- Article
Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy.
- Published in:
- Molecular Syndromology, 2021, v. 12, n. 3, p. 194, doi. 10.1159/000514122
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- Publication type:
- Article
Α case of seronegative autoimmune encephalitis associated with human herpesvirus‐7 (HHV‐7).
- Published in:
- 2022
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- Publication type:
- Case Study
Eyes wide open—an atypical presentation of Miller Fisher syndrome (MFS): case report.
- Published in:
- Egyptian Journal of Neurology, Psychiatry & Neurosurgery, 2022, v. 58, n. 1, p. 1, doi. 10.1186/s41983-022-00451-3
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- Publication type:
- Article
LONG TERM FOLLOW UP OF COMPLETE BLADDER EXSTROPHY REPAIR. A CASE REPORT.
- Published in:
- Folia Medica, 2014, v. 56, n. 1, p. 60, doi. 10.2478/folmed-2014-0010
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- Publication type:
- Article
Incidence and frequency of mucocutaneous exposure and percutaneous injuries in Greek nurses: are they protected enough?
- Published in:
- Balkan Military Medical Review, 2014, v. 17, n. 4, p. 120, doi. 10.5455/bmmr.176132
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- Publication type:
- Article