Detail page

Knowledge Web

Person

Olaf Hiort

Arzt

Name	Olaf Hiort
Place	Lübeck (Wirkungsort) Deutschland
Academic degree	Prof. Dr. med.
Profession	Arzt (characteristic profession) Facharzt für Kinder- und Jugendmedizin
Variant	O. Hiort
Related	Klinik für Kinder- und Jugendmedizin (Lübeck) (Pädiatrische Endokrinologie und Diabetologie)
Record type	Person
GND-Identifier	112321615
Record ID	112321615
Involved in show all Mehr Sicherheit im Umgang mit Varianten der Geschlechtsentwicklung : Online-Kurs gibt Orientierung für Diagnostik und Betreuung Neugeborenes Kind mit auffälligem Genitale : Vorbereitung auf die Facharztprüfung: Fall 122 Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development? Contexts of care for people with differences of sex development : Diversity is still missing in the laboratory routine Is sex still binary? The Role of Genetics in Sex Diversity Development and evaluation of a patient education programme for children, adolescents, and young adults with differences of sex development (DSD) and their parents: study protocol of Empower-DSD Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome Versorgung von Menschen mit Besonderheiten der Geschlechtsentwicklung Intersex, DSD, and the Child’s Well-Being: Changing Perceptions Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE Video Consultation for Parents with a Child Newly Diagnosed with Type 1 Diabetes: A Qualitative Study Pubertal development in 46,XY patients with NR5A1 mutations Access to patient oriented information—a baseline Endo-ERN survey among patients with rare endocrine disorders Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research CPMS–improving patient care in Europe via virtual case discussions Assessing the health-related management of people with differences of sex development Introduction to Endo-ERN–scope and mission Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis Assessing the benefits and challenges of video consultations for the treatment of children with type 1 diabetes – A qualitative study among diabetes professionals Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) Pädiatrische Endokrinologie und Diabetologie Pädiatrische Endokrinologie und Diabetologie : mit 22 Abbildungen und 13 Tabellen Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement Endoscopy and Laparoscopy in Disorders of Sex Development Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome Gesundheitsbezogene Lebensqualität, Selbstwert und Gesundheitsverhalten durchschnittlich 6 Jahre nach einem ambulanten Adipositastherapieprogramm New NR5A1 mutations and phenotypic variations of gonadal dysgenesis Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency  Current models of care for disorders of sex development – results from an International survey of specialist centres Understanding Differences and Disorders of Sex Development (DSD) Understanding differences and disorders of sex development (DSD) : 26 tables Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation Pädiatrische Endokrinologie und Diabetologie Pädiatrische Endokrinologie und Diabetologie ; 64 Tabellen Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome Androgenresistenz : Physiologie und Pathophysiologie der Androgenwirkung Immunhistologische Lokalisation und Verteilung von Östrogenrezeptoren und Sexualhormon bindendem Globulin in normalem und neoplastischem Mammagewebe : ein experimenteller Beitrag zur Diagnostik der Hormonabhängigkeit des Mammakarzinoms

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Olaf Hiort

Mehr Sicherheit im Umgang mit Varianten der Geschlechtsentwicklung : Online-Kurs gibt Orientierung für Diagnostik und Betreuung

Neugeborenes Kind mit auffälligem Genitale : Vorbereitung auf die Facharztprüfung: Fall 122

Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls

Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?

Contexts of care for people with differences of sex development : Diversity is still missing in the laboratory routine

Is sex still binary?

The Role of Genetics in Sex Diversity

Development and evaluation of a patient education programme for children, adolescents, and young adults with differences of sex development (DSD) and their parents: study protocol of Empower-DSD

Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome

Versorgung von Menschen mit Besonderheiten der Geschlechtsentwicklung

Intersex, DSD, and the Child’s Well-Being: Changing Perceptions

Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE

Video Consultation for Parents with a Child Newly Diagnosed with Type 1 Diabetes: A Qualitative Study

Pubertal development in 46,XY patients with NR5A1 mutations

Access to patient oriented information—a baseline Endo-ERN survey among patients with rare endocrine disorders

Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research

CPMS–improving patient care in Europe via virtual case discussions

Assessing the health-related management of people with differences of sex development

Introduction to Endo-ERN–scope and mission

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis

Assessing the benefits and challenges of video consultations for the treatment of children with type 1 diabetes – A qualitative study among diabetes professionals

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

Pädiatrische Endokrinologie und Diabetologie

Pädiatrische Endokrinologie und Diabetologie : mit 22 Abbildungen und 13 Tabellen

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

Endoscopy and Laparoscopy in Disorders of Sex Development

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome

Gesundheitsbezogene Lebensqualität, Selbstwert und Gesundheitsverhalten durchschnittlich 6 Jahre nach einem ambulanten Adipositastherapieprogramm

New NR5A1 mutations and phenotypic variations of gonadal dysgenesis

Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency

Current models of care for disorders of sex development – results from an International survey of specialist centres

Understanding Differences and Disorders of Sex Development (DSD)

Understanding differences and disorders of sex development (DSD) : 26 tables

Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation

Pädiatrische Endokrinologie und Diabetologie

Pädiatrische Endokrinologie und Diabetologie ; 64 Tabellen

Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome

Androgenresistenz : Physiologie und Pathophysiologie der Androgenwirkung

Immunhistologische Lokalisation und Verteilung von Östrogenrezeptoren und Sexualhormon bindendem Globulin in normalem und neoplastischem Mammagewebe : ein experimenteller Beitrag zur Diagnostik der Hormonabhängigkeit des Mammakarzinoms

Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency 