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List of works by Maria New

A girl with 45,X/46,XX Turner syndrome and salt wasting form of congenital adrenal hyperplasia due to regulatory changes

scientific article published on 01 January 2012

A global view of the OCA2-HERC2 region and pigmentation

scientific article

A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita

scientific article published on 21 August 2018

A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.

scientific article published on 15 August 2016

A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance

scientific article published on 20 August 2015

Actions of pituitary hormones beyond traditional targets

scientific article published on 19 March 2018

Adrenal disease in pregnancy

scientific article published on December 2011

Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency.

scientific article published in July 2002

Aldosterone-to-renin ratio as a marker for disease severity in 21-hydroxylase deficiency congenital adrenal hyperplasia

scientific article published on 10 October 2006

An Update on Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia

scientific article published on 08 October 2012

An update of congenital adrenal hyperplasia

scientific article

Anabolic actions of Notch on mature bone

scientific article published on 28 March 2016

Ancient history of congenital adrenal hyperplasia

scientific article published on 16 December 2010

Apparent mineralocorticoid excess and the long term treatment of genetic hypertension

scientific article

Apparent mineralocorticoid excess manifested in an elderly patient with hypothyroidism

scientific article published on 01 April 2007

Ascorbic Acid Treatment in Nephropathie Cystinosis in Identical Twins

scholarly article

Atypical Presentation and Novel StAR Protein Gene Mutation in a 46,XY Female with Lipoid Congenital Adrenal Hyperplasia

scientific article published on January 1, 2011

Beyond Bone Biology: Lessons from Team Science

scientific article published on 10 June 2020

Bilateral laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency

scientific article published on 01 February 2002

Bisphosphonates inactivate human EGFRs to exert antitumor actions

scientific article

Blocking FSH induces thermogenic adipose tissue and reduces body fat.

scientific article published on 24 May 2017

Blocking antibody to the β-subunit of FSH prevents bone loss by inhibiting bone resorption and stimulating bone synthesis

scientific article published on August 20, 2012

Body mass index and age at menarche in an adolescent clinic population

scientific article published on 01 September 2002

Bromodomain Protein BRD4 Is a Transcriptional Repressor of Autophagy and Lysosomal Function

scientific article

CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish children

scientific article

Characterization of insulin resistance syndrome in children and young adults. When to screen for prediabetes?

scientific article published in September 2007

Chemokine (C-C motif) receptor 5 entry inhibitors: new class of drugs for acquired immune deficiency syndrome

scientific article published in May 2008

Clinical Exemplification of HDAC Inhibitors: From Bench to Clinic, and Back Again

article published in 2013

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency

scientific article published on 11 December 2017

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

scientific article published on 22 February 2017

Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature

scientific article

Cognitive and motor development of children with and without congenital adrenal hyperplasia after early-prenatal dexamethasone.

scientific article published on February 2004

Cognitive outcome of offspring from dexamethasone-treated pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency

scientific article

Concomitant secretion of glucocorticoid, androgens, and mineralocorticoid by an adrenocortical carcinoma: case report and review of literature

scientific article published on July 2007

Congenital Adrenal Hyperplasia

scientific article published on 24 April 2015

Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment

scientific article published on 24 April 2015

Congenital Adrenal Hyperplasia: Unresolved Issues.

scientific article

Congenital adrenal hyperplasia and poverty

scientific article published on 01 October 2006

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment

scientific article published on March 2010

Congenital adrenal hyperplasia in adolescents: diagnosis and management

scientific article published on January 2008

Congenital adrenal hyperplasia in adults

scientific article published on 01 January 2009

Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene

scientific article published on November 15, 2011

Description and Defense of Prenatal Diagnosis and Treatment With Low-Dose Dexamethasone for Congenital Adrenal Hyperplasia

scientific article published on September 1, 2010

Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature

scientific article published on October 2006

Effects of adrenal steroids on the bone metabolism of children with congenital adrenal hyperplasia

scientific article

Emerging concepts in the epidemiology, pathophysiology, and clinical care of osteoporosis across the menopausal transition

scientific article published on 05 May 2018

Emerging roles of transcriptional programs in autophagy regulation

scientific article published on 5 October 2017

Epitope-specific monoclonal antibodies to FSHβ increase bone mass

scientific article published on 12 February 2018

Erratum to “Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency” [Mol. Genet. Metabol. 90/4 (2007) 414–421]

scholarly article published in Molecular Genetics and Metabolism

Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

scientific article published in February 2007

Extensive clinical experience: nonclassical 21-hydroxylase deficiency

scientific article

FSH, Bone Mass, Body Fat, and Biological Aging

scientific article published on 01 October 2018

FSIP1 binds HER2 directly to regulate breast cancer growth and invasiveness

scientific article published on 03 July 2017

FSIP1 regulates autophagy in breast cancer

scientific article published on 03 December 2018

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity

scientific article published in August 2005

Fertility in patients with congenital adrenal hyperplasia

scientific article

Fertility in patients with nonclassical congenital adrenal hyperplasia

scientific article published on 01 January 2019

Final Adult Height in Children with Congenital Adrenal Hyperplasia Treated with Growth Hormone

scientific article published on March 30, 2011

First-in-class humanized FSH blocking antibody targets bone and fat

scientific article published on 30 October 2020

Functions of vasopressin and oxytocin in bone mass regulation

scientific article

Gender development in women with congenital adrenal hyperplasia as a function of disorder severity

scientific article published on 11 August 2006

Genetic confirmation for a central role for TNFα in the direct action of thyroid stimulating hormone on the skeleton

scientific article published on May 28, 2013

Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

scientific article published on January 28, 2013

Glucocerebrosidase 2 gene deletion rescues type 1 Gaucher disease

scientific article published on 17 March 2014

Growth Hormone Treatment in Children with Congenital Adrenal Hyperplasia

scientific article published on 01 January 2011

Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

scientific article published on 01 August 2007

HDAC inhibitor-based therapies: can we interpret the code?

scientific article published on 23 October 2012

Human hydroxymethylbilane synthase: Molecular dynamics of the pyrrole chain elongation identifies step-specific residues that cause AIP.

scientific article published on 9 April 2018

Hypertension and adrenal disorders

scientific article published on December 2003

Identification and Validation of Novel Autophagy Regulators Using an Endogenous Readout siGENOME Screen

scientific article published on 01 January 2019

In vitro expression studies of a novel mutation delta299 in a patient affected with apparent mineralocorticoid excess

scientific article

Inactivation of the acid labile subunit gene resulting in insulin-like growth factor deficiency

scientific article published on 01 January 2008

Inborn errors of adrenal steroidogenesis

scientific article published on December 2003

Introduction: Contemporary perspectives on congenital adrenal hyperplasia: impacts on reproduction

scientific article published on 01 January 2019

Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysis

scientific article published on 10 January 2011

Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype

scientific article published on 22 June 2017

Long Range Outcome of Prenatal Treatment

scientific article published on 01 January 2011

Long term outcomes in 46, XX adult patients with congenital adrenal hyperplasia reared as males

scientific article published on 25 April 2016

Long-term growth hormone therapy in an adolescent boy with 45,X/46,XidicY(p11)

scientific article published on 01 November 2009

Low renin hypertension (LRH): shades of John Laragh

scientific article published in 2008

Low-Renin Hypertension of Childhood

scientific article published on 01 June 2011

MDH1 and MPP7 Regulate Autophagy in Pancreatic Ductal Adenocarcinoma

scientific article published on 14 February 2019

Mechanism of glucocerebrosidase activation and dysfunction in Gaucher disease unraveled by molecular dynamics and deep learning

scientific article published on 26 February 2019

Molecular Pathways Controlling Autophagy in Pancreatic Cancer

scientific article

Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia

scientific article published on 31 March 2016

Monogenic low renin hypertension

scientific article

Mutation analysis of the CYP21A2 gene in the Iranian population

scientific article published on 21 October 2011

Mutation of growth hormone receptor in children with Idiopathic Short Stature

scientific article published on 01 December 2008

Nonclassic 21-hydroxylase deficiency

scientific article published on 01 July 2006

Nonclassic 21-hydroxylase deficiency in Croatia

scientific article published in February 2004

Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia

scientific article published on 10 December 2015

Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma

scientific article

Osteoblast regulation via ligand-activated nuclear trafficking of the oxytocin receptor

scientific article

Ovarian carcinoma in a 14-year-old with classical salt-wasting congenital adrenal hyperplasia and bilateral adrenalectomy

scientific article published in May 2015

Oxytocin regulates body composition

scientific article published on 16 December 2019

Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor.

scientific article

Personalised Cancer Medicine: Fulfilling the Promise

Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiency

scientific article published on May 2015

Pituitary-bone connection in skeletal regulation

scientific article

Prenatal Androgenization Affects Gender-Related Behavior But Not Gender Identity in 5–12-year-Old Girls with Congenital Adrenal Hyperplasia

scientific article published on 01 April 2004

Prenatal Diagnosis of Congenital Adrenal Hyperplasia

scientific article published on 31 March 2016

Prenatal diagnosis and treatment of congenital adrenal hyperplasia

scientific article published on 17 October 2006

Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

scientific article published on 03 December 2008

Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

scientific article published on May 2007

Prenatal diagnosis and treatment of congenital adrenal hyperplasia.

scientific article published in December 2006

Prolongation of growth by treatment of 11-hydroxylase deficiency with depot-leuprolide, growth hormone, and hydrocortisone

scientific article published on 01 October 2006

RNAi-mediated silencing of hepatic Alas1 effectively prevents and treats the induced acute attacks in acute intermittent porphyria mice

scientific article

Regulation of bone remodeling by vasopressin explains the bone loss in hyponatremia.

scientific article published on 28 October 2013

Remission of hypertension and electrolyte abnormalities following renal transplantation in a patient with apparent mineralocorticoid excess well documented throughout childhood

scientific article published on 01 January 2014

Reply

scholarly article by Robert G. Lahita et al published January 1988 in Arthritis and Rheumatism

Reply to Graham et al.: In silico atomistic coordinates and molecular dynamics simulation trajectories of the glucocerebrosidase-saposin C complex

scientific article published on 01 June 2019

Report of Fertility in a Woman with a Predominantly 46,XY Karyotype in a Family with Multiple Disorders of Sexual Development

scientific article published on 01 January 2011

Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development

scientific article

Report of fertility in woman with predominantly 46,XY karyotype in family with multiple disorders of sexual development: review of prismatic case

scientific article published on March 2008

Repurposing erectile dysfunction drugs tadalafil and vardenafil to increase bone mass

scientific article published on 08 June 2020

Repurposing of bisphosphonates for the prevention and therapy of nonsmall cell lung and breast cancer

scientific article

Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese children

scientific article published in April 2008

Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess

scientific article published on February 2008

Single-Step, High-Efficiency CRISPR-Cas9 Genome Editing in Primary Human Disease-Derived Fibroblasts

scientific article published on 01 February 2019

Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other

scientific article published on 22 December 2009

Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia

scientific article published on 21 February 2008

Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia

scientific article published on October 1, 2011

Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia

scientific article published on December 2009

Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia

scientific article

Stigma Associated with Classical Congenital Adrenal Hyperplasia in Women's Sexual Lives.

scientific article published on 18 May 2017

Stigma in Medical Settings As Reported Retrospectively by Women With Congenital Adrenal Hyperplasia (CAH) for Their Childhood and Adolescence

scientific article published on 16 May 2016

Structure–phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia

scientific article published on January 28, 2013

Syndrome-Related Stigma in the General Social Environment as Reported by Women with Classical Congenital Adrenal Hyperplasia

scientific article published on 27 September 2016

TLR Adaptor Protein MYD88 Mediates Sensitivity to HDAC Inhibitors via a Cytokine-Dependent Mechanism

scientific article published on 12 October 2016

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency

scientific article published on 03 August 2010

The Recalled Childhood Gender Questionnaire-Revised: a psychometric analysis in a sample of women with congenital adrenal hyperplasia

scientific article published in November 2006

The Role of Autophagy in Pancreatic Cancer-Recent Advances

scientific article published on 28 December 2019

The distribution and most recent common ancestor of the 17q21 inversion in humans

scientific article (publication date: 12 February 2010)

The myokine irisin increases cortical bone mass.

scientific article

Thymic Carcinoid Presenting With Cushing's Syndrome in a 17-Year-Old Boy: A Case Report and Review of the Literature

scientific article published on July 18, 2011

Treatment with growth hormone and luteinizing hormone releasing hormone analog improves final adult height in children with congenital adrenal hyperplasia

scientific article published on 29 March 2005

Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11 β -Hydroxylase Deficiency

scientific article

Two novel mutations found in a patient with 17alpha-hydroxylase enzyme deficiency

scientific article published on 18 July 2006

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases

scientific article published on 8 December 2016

Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency).

scientific article published on May 2005

Vindication of prenatal diagnosis and treatment of congenital adrenal hyperplasia with low-dose dexamethasone

scientific article published in December 2010

WITHDRAWN: Low renin hypertension (LRH): shades of John Laragh

retracted scientific article published on 18 March 2008