Found: 16
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Subcutaneous immunoglobulin in infantile chronic inflammatory demyelinating polyneuropathy: A case report.
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- Journal of Pediatric Neurosciences, 2019, v. 14, n. 1, p. 38, doi. 10.4103/JPN.JPN_132_18
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- Article
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases.
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- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. N.PAG, doi. 10.1186/s13052-020-00937-x
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- Article
Antimicrobial activity and chemical composition of essential oils from sicilian aromatic plants.
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- Flavour & Fragrance Journal, 1993, v. 8, n. 6, p. 331, doi. 10.1002/ffj.2730080608
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- Article
14q32.3-qter trisomic segment: a case report and literature review.
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- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0265-5
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- Article
Ganglioglioma of the Spinal Cord in Neurofibromatosis Type 1.
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- Pediatric Neurosurgery, 2013, v. 49, n. 1, p. 50, doi. 10.1159/000355249
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- Article
SMC1A epilepsy syndrome: clinical data from a large international cohort.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 7, p. 1, doi. 10.1002/ajmg.a.63577
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- Article
Celiac disease prevalence and predisposing‐HLA in a cohort of 93 Williams‐Beuren syndrome patients.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 1, p. 84, doi. 10.1002/ajmg.a.62990
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- Article
Pulmonary function in Williams–Beuren syndrome: Spirometric data of 22 Italian patients.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 390, doi. 10.1002/ajmg.a.61966
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- Article
Complex nutritional deficiencies in a large cohort of Italian patients with Cornelia de Lange syndrome spectrum.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 9, p. 2094, doi. 10.1002/ajmg.a.61749
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- Article
Nissen fundoplication in Cornelia de Lange syndrome spectrum: Who are the potential candidates?
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 7, p. 1697, doi. 10.1002/ajmg.a.61625
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- Article
Anthropometric characteristics of newborns with Prader–Willi syndrome.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 10, p. 2067, doi. 10.1002/ajmg.a.61304
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- Article
Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 2, p. 546, doi. 10.1002/ajmg.a.38057
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- Article
Cervical spine malformation in cornelia de lange syndrome: A report of three patients.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 6, p. 1520, doi. 10.1002/ajmg.a.36457
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- Article
Collagenopathy with a phenotype resembling silver-russell syndrome phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 10, p. 2681, doi. 10.1002/ajmg.a.36093
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- Article
Two cases of hepatic adenomas in patients with wolf-hirschhorn syndrome: A new rare complication?
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 7, p. 1759, doi. 10.1002/ajmg.a.35966
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- Article
A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1401, doi. 10.1002/ajmg.a.35875
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- Article