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Orphanet Journal of Rare Diseases
|
December 9, 2024
Quality of care for people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Corrigendum to: Clinical spectrum and management of imprinting disorders
Miriam Elbracht, Gerhard Binder, Olaf Hiort, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2011
Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5
Şenay Savaş Erdeve, Merih Berberoğlu, Zeynep Şıklar, et al.
Journal of Pediatric and Adolescent Gynecology
|
May 15, 2012
46,XY karyotype in a female phenotype fetus: a challenging diagnosis
Gianni Russo, Alessandra di Lascio, Matilde Ferrario, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Contexts of care for people with differences of sex development: Diversity is still missing in the laboratory routine
Alexandra E Kulle, Martina Jürgensen, Ulla Döhnert, et al.
European Journal of Pediatrics
|
June 13, 2008
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapy
Verena M Wagner, Britta Kremke, Olaf Hiort, et al.
Genome Biology
|
June 13, 2003
Differential gene-expression patterns in genital fibroblasts of normal males and 46,XY females with androgen insensitivity syndrome: evidence for early programming involving the androgen receptor
Paul-Martin Holterhus, Olaf Hiort, Janos Demeter, et al.
European Journal of Pediatrics
|
January 29, 2014
Health-related quality of life in children with disorders of sex development (DSD)
Martina Jürgensen, Anke Lux, Sebastian Benedikt Wien, et al.
Orvosi Hetilap
|
November 30, 2006
[Incomplete androgen insensitivity]
Andrea Luczay, János Sólyom, Olaf Hiort, et al.
Endocrine Connections
|
March 9, 2026
Assessment of the 5 Year Evaluation for 1st call members of the European Reference Network on Rare Endocrine Conditions (Endo-ERN)
Emily K White, Tessa de Bruin, Olaf Hiort, et al.
Page
of 20
Search research articles
Search
Showing results (61-70 of 195) with videos related to
Sort By:
Page
of 20
Orphanet Journal of Rare Diseases
|
December 9, 2024
Quality of care for people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Corrigendum to: Clinical spectrum and management of imprinting disorders
Miriam Elbracht, Gerhard Binder, Olaf Hiort, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2011
Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5
Şenay Savaş Erdeve, Merih Berberoğlu, Zeynep Şıklar, et al.
Journal of Pediatric and Adolescent Gynecology
|
May 15, 2012
46,XY karyotype in a female phenotype fetus: a challenging diagnosis
Gianni Russo, Alessandra di Lascio, Matilde Ferrario, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Contexts of care for people with differences of sex development: Diversity is still missing in the laboratory routine
Alexandra E Kulle, Martina Jürgensen, Ulla Döhnert, et al.
European Journal of Pediatrics
|
June 13, 2008
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapy
Verena M Wagner, Britta Kremke, Olaf Hiort, et al.
Genome Biology
|
June 13, 2003
Differential gene-expression patterns in genital fibroblasts of normal males and 46,XY females with androgen insensitivity syndrome: evidence for early programming involving the androgen receptor
Paul-Martin Holterhus, Olaf Hiort, Janos Demeter, et al.
European Journal of Pediatrics
|
January 29, 2014
Health-related quality of life in children with disorders of sex development (DSD)
Martina Jürgensen, Anke Lux, Sebastian Benedikt Wien, et al.
Orvosi Hetilap
|
November 30, 2006
[Incomplete androgen insensitivity]
Andrea Luczay, János Sólyom, Olaf Hiort, et al.
Endocrine Connections
|
March 9, 2026
Assessment of the 5 Year Evaluation for 1st call members of the European Reference Network on Rare Endocrine Conditions (Endo-ERN)
Emily K White, Tessa de Bruin, Olaf Hiort, et al.
Page
of 20