Alexander L. Jorge
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 115 publications
Once-weekly somapacitan enhances linear growth in girls with Turner syndrome: a randomized controlled phase 3 study.
Journal: The Journal of clinical endocrinology and metabolism
Published: May 09, 2026
Genetic testing in "Mild Growth Hormone Deficiency".
Journal: European journal of endocrinology
Published: February 03, 2026
International guideline on genetic testing of children with short stature.
Journal: European journal of endocrinology
Published: January 03, 2026
International guideline on genetic testing of children with short stature.
Journal: European journal of endocrinology
Published: January 03, 2026
Bi-allelic WDHD1 variants cause microcephalic primordial dwarfism.
Journal: American journal of human genetics
Published: December 18, 2025
Diagnostic yield of genetic testing in children with short stature: a systematic review.
Journal: European journal of endocrinology
Published: October 16, 2025
Once-weekly somapacitan in children with Noonan syndrome: randomized controlled phase 3 trial.
Journal: European journal of endocrinology
Published: July 25, 2025
Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series.
Journal: Archives of endocrinology and metabolism
Published: May 14, 2025
Exome sequencing of patients with syndromic tall stature reveals four novel candidate genes.
Journal: Endocrine connections
Published: March 10, 2025
AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions.
Journal: American journal of medical genetics. Part A
Published: February 27, 2025
Sitosterolemia caused by compound heterozygosis of 2 allelic variants in the ABCG5 gene-21 years of follow-up.
Journal: Journal of clinical lipidology
Published: February 01, 2025
Last Updated: 09/26/2026