Works matching IS 09185739 AND DT 2024 AND VI 33 AND IP 1
Results: 7
A novel missense variant of FGD1 disrupts critical cysteine residues of the FYVE domain in Japanese siblings with Aarskog-Scott syndrome.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 39, doi. 10.1297/cpe.2023-0027
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- Article
Pitfalls in estradiol measurement by electrochemiluminescence immunoassay: A case study of a prepubertal girl with a falsely elevated serum estradiol level.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 35, doi. 10.1297/cpe.2023-0054
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- Article
Switching to burosumab from conventional therapy in siblings with relatively well-controlled X-linked hypophosphatemia.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 27, doi. 10.1297/cpe.2023-0043
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- Article
A thyroid adenoma in a pubertal male with thyroxine-binding globulin deficiency.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 23, doi. 10.1297/cpe.2023-0031
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- Article
A novel variant of IGSF1 in siblings with congenital central hypothyroidism whose diagnosis was prompted by school health checkups.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 17, doi. 10.1297/cpe.2023-0046
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- Article
A Japanese school urine screening program led to the diagnosis of KCNJ11-MODY: A case report.
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- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 12, doi. 10.1297/cpe.2023-0037
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- Article
GH therapy in children with juvenile idiopathic arthritis: a four-decade review.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 1, p. 1, doi. 10.1297/cpe.2023-0036
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- Article