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List of works by Svetlana Lajic

A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

scientific article published on 01 June 1997

A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain of human steroid 21-hydroxylase

scientific article published on 01 February 1999

An intron 1 splice mutation and a nonsense mutation (W23X) in CYP21 causing severe congenital adrenal hyperplasia

scientific article published on 01 August 1996

Assessment of medication adherence in children and adults with congenital adrenal hyperplasia and the impact of knowledge and self-management

scientific article published on 21 December 2020

Assisted large fragment insertion by Red/ET-recombination (ALFIRE)--an alternative and enhanced method for large fragment recombineering.

scientific article published on 21 May 2007

Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.

scientific article published on 21 November 2006

Cognitive functions in children at risk for congenital adrenal hyperplasia treated prenatally with dexamethasone

scientific article

Cognitive impairment in adolescents and adults with congenital adrenal hyperplasia

scientific article published on 3 August 2017

Deficient cardiovascular stress reactivity predicts poor executive functions in adults with attention-deficit/hyperactivity disorder

scientific article published on 05 July 2010

Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)

scientific article published on 01 April 1999

Epigenetic Alterations Associated With Early Prenatal Dexamethasone Treatment

scientific article published on 12 December 2018

Evaluation of behavioral problems after prenatal dexamethasone treatment in Swedish children and adolescents at risk of congenital adrenal hyperplasia.

scientific article published on 31 January 2018

Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia

scientific article

Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects.

scientific article published on 19 September 2016

Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH

scientific article published on 01 May 2012

Functional studies of two novel and two rare mutations in the 21-hydroxylase gene

article

Gender role behaviour in prenatally dexamethasone-treated children at risk for congenital adrenal hyperplasia--a pilot study

scientific article

High self-perceived stress and many stressors, but normal diurnal cortisol rhythm, in adults with ADHD (attention-deficit/hyperactivity disorder).

scientific article published on 31 December 2008

How can molecular biology contribute to the management of congenital adrenal hyperplasia?

scientific article published in January 2000

In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

scientific article published on 7 July 2014

Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patients

scientific article published in April 2008

Long-term follow-up of prenatally treated children at risk for congenital adrenal hyperplasia: does dexamethasone cause behavioural problems?

scientific article published on 25 June 2008

Long-term outcome of prenatal dexamethasone treatment of 21-hydroxylase deficiency

scientific article

Long-term outcome of prenatal treatment of congenital adrenal hyperplasia

scientific article published on January 2008

Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stability

scientific article published on 01 March 1998

Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia

scientific article published on 28 December 2004

Novel mutations in CYP21 detected in individuals with hyperandrogenism.

scientific article published in June 2002

Prenatal Treatment of Congenital Adrenal Hyperplasia: Long-Term Effects of Excess Glucocorticoid Exposure

scientific article published on 09 May 2018

Prenatal dexamethasone treatment in the context of at risk CAH pregnancies: Long-term behavioral and cognitive outcome

scientific article published in March 2018

Prenatal dexamethasone treatment of children at risk for congenital adrenal hyperplasia: the Swedish experience and standpoint

scientific article published in June 2012

Prenatal diagnosis and treatment of adrenogenital syndrome. Prevent virilization of female fetuses

scientific article published in December 1997

Rescue of defective G protein-coupled receptor function in vivo by intermolecular cooperation.

scientific article

Retraction notice to"Evaluation of behavioral problems after prenatal dexamethasone treatment in Swedish adolescents at risk of CAH" [Hormones and Behavior 85C (2016) 5-11]

scientific article published on 01 July 2018

Sex-Dimorphic Effects of Prenatal Treatment With Dexamethasone.

scientific article published on 2 August 2016

Steroid 21-hydroxylase in the kidney: Demonstration of levels of messenger RNA which correlate with the level of activity

scientific article published on 01 February 1995

The Success of a Screening Program Is Largely Dependent on Close Collaboration between the Laboratory and the Clinical Follow-Up of the Patients

scientific article published on 26 August 2020

Update on the Swedish Newborn Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

scientific article published on 28 August 2020

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