Susanne E. Stalman
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome.
Journal: Frontiers in endocrinology
Published: May 26, 2022
Novel Clinical Criteria Allow Detection of Short Stature Homeobox-Containing Gene Haploinsufficiency Caused by Either Gene or Enhancer Region Defects.
Journal: Hormone research in paediatrics
Published: October 04, 2019
Genetic Analyses in Small-for-Gestational-Age Newborns.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 18, 2017
Diagnostic Work-up and Follow-up in Children with Tall Stature: A Simplified Algorithm for Clinical Practice.
Journal: Journal of clinical research in pediatric endocrinology
Published: January 19, 2016
Growth failure in adolescents: etiology, the role of pubertal timing and most useful criteria for diagnostic workup.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 03, 2015
Application of the Dutch, Finnish and British Screening Guidelines in a Cohort of Children with Growth Failure.
Journal: Hormone research in paediatrics
Published: May 04, 2015
Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome
Journal: Nederlands tijdschrift voor geneeskunde
Published: April 23, 2015
Psychometric performance of the Quality of Life in Short Stature Youth (QoLISSY) questionnaire in the Netherlands.
Journal: European journal of pediatrics
Published: March 28, 2015
Positive effect of growth hormone treatment in maternal uniparental disomy chromosome 14.
Journal: Clinical endocrinology
Published: March 26, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026