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Pasireotide treatment for severe congenital hyper-insulinism due to a homozygous ABCC8 mutation

Subjects: medicine.medical_specialty; Endocrinology, Diabetes and Metabolism; medicine.medical_treatment

  • Source: Annals of pediatric endocrinology & metabolism, 26(4), 278-283. KOREAN SOC PEDIATRIC ENDOCRINOLOGYAnnals of pediatric endocrinology & metabolism, 26(4), 278-283. Korean society of pediatric

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Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study

Subjects: medicine.medical_specialty; Pediatrics; Endocrinology, Diabetes and Metabolism

  • Source: The Journal of clinical endocrinology and metabolism, 106(11), E4487-E4496. The Endocrine SocietyJournal of clinical endocrinology and metabolism, 106(11), E4487-E4496. The Endocrine Society

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Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasia

Subjects: Male; Pediatrics; medicine.medical_specialty

  • Source: Archives of Disease in Childhood, 104(7), 653-657. BMJ Publishing GroupArchives of Disease in Childhood, 104, 653-657Archives of Disease in Childhood, 104(7), 653-657. BMJ PUBLISHING

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  • 1-10 of  17 نتائج ل ""Mirjam E. van Albada""