Detailansicht

Wissensnetz

Person

Daniela Choukair (1972-)

Ärztin

Name	Daniela Choukair
Zeit	1972- (Lebensdaten)
Ort	Göttingen (Geburtsort) Heidelberg (Wirkungsort) Deutschland
Akademischer Grad bzw. Titel	PD Dr. med.
Beruf	Ärztin (charakteristischer Beruf)
Variante	Daniela Kiepe (Geburtsname) (früherer Name)
Beziehung	Klinikum Heidelberg
Weitere Angaben	Funktionsoberärztin, Klinik Kinderheilkunde I, Zentrum für Kinder- und Jugendmedizin Heidelberg, Universitätsklinikum Heidelberg
Datensatztyp	Person
GND-Nummer	120713381
Datensatz-ID	120713381
Beteiligt an alle anzeigen Resource utilization and costs of transitioning from pediatric to adult care for patients with chronic autoinflammatory and autoimmune disorders Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project) Resource use and costs of transitioning from pediatric to adult care for patients with chronic kidney disease Transition for adolescents with a rare disease: results of a nationwide German project Topical glucocorticoid application causing iatrogenic Cushing’s syndrome followed by secondary adrenal insufficiency in infants: two case reports Near-Adult Heights and Adult Height Predictions Using Automated and Conventional Greulich–Pyle Bone Age Determinations in Children with Chronic Endocrine Diseases Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee Kidney re-transplantation in a child across the barrier of persisting angiotensin II type I receptor antibodies Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency Analysis of the functional muscle–bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomography Virilization of a Young Girl Caused by Concomitant Ectopic and Intra-Adrenal Adenomas of the Adrenal Cortex The IGF/IGFBP system in relation to macroscopic bone architecture in pediatric renal transplant patients Ventrikelweitenmessung mit transkraniellem Ultraschall

Hinweis

Die Betaversion beinhaltet noch nicht alle Funktionen und Informationen des Katalogs des DNB-Portals. Falls Sie Informationen vermissen oder ein Medium bestellen wollen, besuchen Sie bitte die entsprechende Seite im Katalog des DNB-Portals über folgenden Link:

Katalog der Deutschen Nationalbibliothek

Daniela Choukair (1972-)

Resource utilization and costs of transitioning from pediatric to adult care for patients with chronic autoinflammatory and autoimmune disorders

Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)

Resource use and costs of transitioning from pediatric to adult care for patients with chronic kidney disease

Transition for adolescents with a rare disease: results of a nationwide German project

Topical glucocorticoid application causing iatrogenic Cushing’s syndrome followed by secondary adrenal insufficiency in infants: two case reports

Near-Adult Heights and Adult Height Predictions Using Automated and Conventional Greulich–Pyle Bone Age Determinations in Children with Chronic Endocrine Diseases

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

An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee

Kidney re-transplantation in a child across the barrier of persisting angiotensin II type I receptor antibodies

Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism

Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency

Analysis of the functional muscle–bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomography

Virilization of a Young Girl Caused by Concomitant Ectopic and Intra-Adrenal Adenomas of the Adrenal Cortex

The IGF/IGFBP system in relation to macroscopic bone architecture in pediatric renal transplant patients

Ventrikelweitenmessung mit transkraniellem Ultraschall