List of works - Guy Van Vliet

A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations

article

A high prevalence of dual thyroid ectopy in congenital hypothyroidism: evidence for insufficient signaling gradients during embryonic thyroid migration or for the polyclonal nature of the thyroid gland?

scientific article published on 28 March 2012

A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene

scientific article (publication date: May 1997)

A search for variables predicting cortisol response to low-dose corticotropin stimulation following supraphysiological doses of glucocorticoids

scientific article published on 12 February 2013

Abstracts Of The Meeting On Obesity Organized By The Contact Groups « Hormones » and « Nutrition » of Frsm/Fwgo On February 23, 1985 In Brussels Effect Of Growth Hormone Releasing Factor (Grf) On Plasma Growth Hormone (Gh) And Prolactin (Prl) Levels

scientific article published on 01 January 1985

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

scientific article

Androgens and fetal growth.

scientific article published in January 1998

Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency.

scientific article published on 27 March 2007

Are guidelines for glucocorticoid coverage in adrenal insufficiency currently followed?

scientific article published on 30 October 2010

Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted? A debate.

scientific article

Association of adrenal insufficiency with insulin-dependent diabetes mellitus in a patient with inactivating mutations in nicotinamide nucleotide transhydrogenase: a phenocopy of the animal model.

scientific article

Autonomous adenomas caused by somatic mutations of the thyroid-stimulating hormone receptor in children.

scientific article published on 30 January 2014

Avoiding the Overdiagnosis of Congenital Hypothyroidism in Premature Newborns

scientific article published on 16 July 2019

Bioinactive ACTH causing glucocorticoid deficiency

scientific article

Cause of dwarfism in Mauriac syndrome ⬇️

scientific article published on 01 May 1981

Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia

scientific article published on 25 October 2020

Clinical case seminar in pediatric thyroid disease.

scientific article published on 29 August 2014

Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism.

scientific article published in November 2006

Cognition and behavior at school entry in children with congenital hypothyroidism treated early with high-dose levothyroxine

scientific article

Cold thyroid nodules in childhood: is surgery always necessary?

scientific article published on 01 July 1987

Comparison of adolescents with Klinefelter syndrome according to the circumstances of diagnosis: amniocentesis versus clinical signs

scientific article published on 18 August 2009

Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism

scientific article published in April 2010

Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage.

scientific article

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained byTPITGene Mutations

scientific article published on 21 December 2004

Congenital hypopituitarism: results of pituitary stimulation tests and of magnetic resonance imaging in a newborn girl

scientific article published in March 1992

Congenital hypothyroidism

scientific article published on 01 September 2006

Congenital hypothyroidism: from paracelsus to molecular diagnosis

scientific article

Congenital hypothyroidism: look at the whole patient! Editorial comment on the paper by El Kholy et al. in this issue

scientific article published on 20 June 2007

Conserved Telomere Length in Human Ectopic Thyroids: An Argument Against Premature Differentiation Causing Arrested Migration

scientific article published on July 2015

Contribution of thyroid ultrasound and serum calcitonin to the diagnosis of congenital hypothyroidism

scientific article published on February 1990

Counselling of a couple faced with a prenatal diagnosis of Klinefelter syndrome

scientific article published on 25 February 2011

Decreased growth hormone response to glucagon in infants after an apnea of infancy

scientific article published on 01 March 1998

Decreased growth hormone response to growth hormone-releasing hormone in Turner's syndrome: relation to body weight and adiposity.

scientific article published in July 1991

Decreasing sex difference in birth weight

scientific article published in July 2009

Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing

scientific article published on 28 April 2016

Development of the thyroid gland: lessons from congenitally hypothyroid mice and men.

scientific article

Diagnosis, treatment and outcome of congenital hypothyroidism.

scientific article published on 29 August 2014

Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology.

scientific article published in September 2002

Discovery of a fetal goiter on prenatal ultrasound in women treated for Graves' disease: first, do no harm

scientific article published on 11 July 2011

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

scientific article

Does growth-hormone supplementation affect adult height in Turner's syndrome?

scientific article published on July 1996

Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations.

scientific article published on 14 November 2015

Effect of growth hormone-releasing factor on plasma growth hormone, prolactin and somatomedin C in hypopituitary and short normal children

scientific article published on 01 January 1985

Evaluation and significance of the degree of pituitary-gonadal inhibition during intranasal administration of buserelin.

scientific article

Experience With Store-and-Forward Consultations in Providing Access to Pediatric Endocrine Consultations in Low- and Middle-Income Countries

scientific article published on 25 September 2019

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

scientific article published on 28 June 2013

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

scientific article published on 01 December 2009

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism.

scientific article published in December 2009

Growth Hormone Supplementation and Psychosocial Functioning to Adult Height in Turner Syndrome: A Questionnaire Study of Participants in the Canadian Randomized Trial

article

Growth hormone supplementation in Turner's syndrome

scientific article published on 01 December 1998

Growth-stimulating effects of human growth hormone therapy in patients with Turner syndrome

scientific article published on 01 December 1986

Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: Further delineation and review

article

Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

scientific article

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

scientific article

How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?

scientific article published on 3 January 2007

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

scientific article

Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruption

scientific article published in February 2002

Hypothalamo-pituitary dysfunction in congenital toxoplasmosis

scientific article published on 01 August 1989

IGF-I transcript levels in whole-liver tissue, in freshly isolated hepatocytes, and in cultured hepatocytes from lean and obese Zucker rats.

scientific article published in January 2003

Impact of patient characteristics and clinical factors on the decision to initiate growth hormone treatment in Turner syndrome.

scientific article published on 30 September 2008

Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism ⬇️

scientific article published on 09 October 2009

Inhibition of growth hormone response in angiomatous lymphoid hamartoma

scientific article published on 01 March 1982

Interpreting Minor Variations in Thyroid Function or Echostructure: Treating Patients, Not Numbers or Images.

scientific article published on 24 June 2015

Is the incidence of congenital hypothyroidism really increasing? A 20-year retrospective population-based study in Québec.

scientific article

Is ultrasonography useful in predicting thyroid cancer in children with thyroid nodules and apparently benign cytopathologic features?

scientific article

Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene

scientific article

Leydig cell tumors in children: contrasting clinical, hormonal, anatomical, and molecular characteristics in boys and girls

scientific article published on 23 June 2012

Longitudinal study of thyroid function in Down's syndrome in the first two decades

scientific article published on 01 November 2005

Lost and found testes: the importance of the hCG stimulation test and other testicular markers to confirm a surgical declaration of anorchia

scientific article published on 30 July 2004

Low somatomedin-C (Sm-C) concentrations measured by direct radioimmunoassay in patients with chronic renal failure.

scientific article published in January 1987

Meeting report: measuring endocrine-sensitive endpoints within the first years of life.

journal article published in 2008

Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype

scientific article published in September 2009

Muscle-bone characteristics in children with Prader-Willi syndrome.

scientific article

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism

scientific article

Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

scientific article

Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.

scientific article published on 17 June 2008

Non-immune goiter and hypothyroidism in a 19-week fetus: a plea for conservative treatment

scientific article published on 20 March 2010

Normal minipuberty of infancy in boys with Prader-Willi syndrome

scientific article published on 01 December 2006

Outcome after bariatric surgery in two adolescents with hypothalamic obesity following treatment of craniopharyngioma

scientific article published on 01 September 2009

Outcome in three siblings with antibody-mediated transient congenital hypothyroidism ⬇️

scientific article published on 01 August 1995

Panhypopituitarism without diabetes insipidus: magnetic resonance imaging of pituitary stalk transection

scientific article published on 01 January 1990

Partnering with parents to disclose Klinefelter syndrome to their child

scientific article published on 19 December 2015

Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.

scientific article published on 8 December 2010

Plasma gonadotropin values in prepubertal cryptorchid boys: Similar increase of FSH secretion in uni- and bilateral cases ⬇️

scientific article published on 01 August 1980

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

scientific article published on 24 August 2007

Possible non-Mendelian mechanisms of thyroid dysgenesis.

scientific article published on January 2007

Premature Ovarian Failure in French Canadian Leigh Syndrome

scientific article published on 08 March 2017

Prevention of intellectual disability through screening for congenital hypothyroidism: how much and at what level?

scientific article published on 17 January 2011

Primary adrenal insufficiency in children: twenty years experience at the Sainte-Justine Hospital, Montreal

scientific article

Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies

scientific article published on 20 November 2007

Quality of referral of short children to the paediatric endocrinologist and impact of a fax communication system

scientific article published on December 2013

Random variability in congenital hypothyroidism from thyroid dysgenesis over 16 years in Québec.

scientific article

Redefining congenital hypothyroidism?

scientific article published on 04 December 2020

Reference intervals for free thyroxine, total triiodothyronine, thyrotropin and thyroglobulin for Quebec newborns, children and teenagers

scientific article published in April 2004

Reply

Retrospective study of the potential benefits and adverse events during growth hormone treatment in children with Prader-Willi syndrome

scientific article published on 23 September 2008

Rising serum thyroxine levels and chorea in graves' disease

scientific article published on 06 January 2013

Role for tissue-dependent methylation differences in the expression of FOXE1 in nontumoral thyroid glands

scientific article published on 19 March 2014

Screening for neonatal endocrinopathies: rationale, methods and results

scientific article published on February 2004

Severe cortisol deficiency associated with reversible growth hormone deficiency in two infants: what is the link?

scientific article published on 13 July 2011

Sex-specific impact of congenital hypothyroidism due to thyroid dysgenesis on skeletal maturation in term newborns

scientific article published in May 2003

Sexual dimorphism of thyroid function in newborns with congenital hypothyroidism

scientific article

Similar age-dependent levothyroxine requirements of schoolchildren with congenital or acquired hypothyroidism.

scientific article published on 9 February 2016

Somatic mutations are not observed by exome sequencing of lymphocyte DNA from monozygotic twins discordant for congenital hypothyroidism due to thyroid dysgenesis.

scientific article published on 23 September 2014

Studies with growth hormone releasing factor in children: diagnostic and therapeutic implications

scientific article published on January 1988

Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome.

scientific article

Sudden death in growth hormone-treated children with Prader-Willi syndrome

scientific article published on January 2004

The changing epidemiology of congenital hypothyroidism: fact or artifact?

scientific article published on 16 May 2014

The continuing health burden of congenital hypothyroidism in the era of neonatal screening

scientific article published on 01 June 2011

Therapeutic approach of fetal thyroid disorders

scientific article published on 07 May 2010

Thyroid dyshormonogenesis: severe hypothyroidism after normal neonatal thyroid stimulating hormone screening

scientific article published on 01 March 1992

Thyroid function from birth to adolescence in Prader-Willi syndrome.

scientific article published on 25 April 2013

Thyroid scintigraphy in children and adolescents with Hashimoto disease

scientific article published on 01 December 1995

Total synthesis of insulin-like growth factor I (somatomedin C).

scientific article published on April 1983

Treating congenital hypothyroidism--which levothyroxine?

scientific article published on 05 March 2013

Treating fetal thyroid and adrenal disorders through the mother

scientific article

Treatment of Turner syndrome with growth hormone

scientific article published on 01 April 1993

Treatment of central precocious puberty with an intranasal analogue of GnRH (Buserelin)

scientific article published on 01 November 1987

Treatment of congenital hypothyroidism

scientific article

Twenty years later: a reevaluation of the contribution of plasma thyroglobulin to the diagnosis of thyroid dysgenesis in infants with congenital hypothyroidism

scientific article published on 01 September 2004

Undetectable AMH at 3 days of age: a clue to bilateral anorchia

scientific article published on 26 August 2010

Variation by Ethnicity in the Prevalence of Congenital Hypothyroidism Due to Thyroid Dysgenesis ⬇️

scientific article published on November 8, 2010

Very low birth weight newborns do not need repeat screening for congenital hypothyroidism

scientific article published in March 2002

Whole-exome sequencing: opportunities in pediatric endocrinology

scientific article published on 01 January 2014

Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism

scientific article published on 31 May 2019

List of works by Guy Van Vliet

A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations

A high prevalence of dual thyroid ectopy in congenital hypothyroidism: evidence for insufficient signaling gradients during embryonic thyroid migration or for the polyclonal nature of the thyroid gland?

A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene

A search for variables predicting cortisol response to low-dose corticotropin stimulation following supraphysiological doses of glucocorticoids

Abstracts Of The Meeting On Obesity Organized By The Contact Groups « Hormones » and « Nutrition » of Frsm/Fwgo On February 23, 1985 In Brussels Effect Of Growth Hormone Releasing Factor (Grf) On Plasma Growth Hormone (Gh) And Prolactin (Prl) Levels

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

Androgens and fetal growth.

Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency.

Are guidelines for glucocorticoid coverage in adrenal insufficiency currently followed?

Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted? A debate.

Association of adrenal insufficiency with insulin-dependent diabetes mellitus in a patient with inactivating mutations in nicotinamide nucleotide transhydrogenase: a phenocopy of the animal model.

Autonomous adenomas caused by somatic mutations of the thyroid-stimulating hormone receptor in children.

Avoiding the Overdiagnosis of Congenital Hypothyroidism in Premature Newborns

Bioinactive ACTH causing glucocorticoid deficiency

Cause of dwarfism in Mauriac syndrome ⬇️

Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia

Clinical case seminar in pediatric thyroid disease.

Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism.

Cognition and behavior at school entry in children with congenital hypothyroidism treated early with high-dose levothyroxine

Cold thyroid nodules in childhood: is surgery always necessary?

Comparison of adolescents with Klinefelter syndrome according to the circumstances of diagnosis: amniocentesis versus clinical signs

Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism

Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage.

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained byTPITGene Mutations

Congenital hypopituitarism: results of pituitary stimulation tests and of magnetic resonance imaging in a newborn girl

Congenital hypothyroidism

Congenital hypothyroidism: from paracelsus to molecular diagnosis

Congenital hypothyroidism: look at the whole patient! Editorial comment on the paper by El Kholy et al. in this issue

Conserved Telomere Length in Human Ectopic Thyroids: An Argument Against Premature Differentiation Causing Arrested Migration

Contribution of thyroid ultrasound and serum calcitonin to the diagnosis of congenital hypothyroidism

Counselling of a couple faced with a prenatal diagnosis of Klinefelter syndrome

Decreased growth hormone response to glucagon in infants after an apnea of infancy

Decreased growth hormone response to growth hormone-releasing hormone in Turner's syndrome: relation to body weight and adiposity.

Decreasing sex difference in birth weight

Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing

Development of the thyroid gland: lessons from congenitally hypothyroid mice and men.

Diagnosis, treatment and outcome of congenital hypothyroidism.

Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology.

Discovery of a fetal goiter on prenatal ultrasound in women treated for Graves' disease: first, do no harm

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

Does growth-hormone supplementation affect adult height in Turner's syndrome?

Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations.

Effect of growth hormone-releasing factor on plasma growth hormone, prolactin and somatomedin C in hypopituitary and short normal children

Evaluation and significance of the degree of pituitary-gonadal inhibition during intranasal administration of buserelin.

Experience With Store-and-Forward Consultations in Providing Access to Pediatric Endocrine Consultations in Low- and Middle-Income Countries

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism.

Growth Hormone Supplementation and Psychosocial Functioning to Adult Height in Turner Syndrome: A Questionnaire Study of Participants in the Canadian Randomized Trial

Growth hormone supplementation in Turner's syndrome

Growth-stimulating effects of human growth hormone therapy in patients with Turner syndrome

Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: Further delineation and review

Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruption

Hypothalamo-pituitary dysfunction in congenital toxoplasmosis

IGF-I transcript levels in whole-liver tissue, in freshly isolated hepatocytes, and in cultured hepatocytes from lean and obese Zucker rats.

Impact of patient characteristics and clinical factors on the decision to initiate growth hormone treatment in Turner syndrome.

Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism ⬇️

Inhibition of growth hormone response in angiomatous lymphoid hamartoma

Interpreting Minor Variations in Thyroid Function or Echostructure: Treating Patients, Not Numbers or Images.

Is the incidence of congenital hypothyroidism really increasing? A 20-year retrospective population-based study in Québec.

Is ultrasonography useful in predicting thyroid cancer in children with thyroid nodules and apparently benign cytopathologic features?

Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene

Leydig cell tumors in children: contrasting clinical, hormonal, anatomical, and molecular characteristics in boys and girls

Longitudinal study of thyroid function in Down's syndrome in the first two decades

Lost and found testes: the importance of the hCG stimulation test and other testicular markers to confirm a surgical declaration of anorchia

Low somatomedin-C (Sm-C) concentrations measured by direct radioimmunoassay in patients with chronic renal failure.

Meeting report: measuring endocrine-sensitive endpoints within the first years of life.

Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype

Muscle-bone characteristics in children with Prader-Willi syndrome.

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism

Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.

Non-immune goiter and hypothyroidism in a 19-week fetus: a plea for conservative treatment

Normal minipuberty of infancy in boys with Prader-Willi syndrome

Outcome after bariatric surgery in two adolescents with hypothalamic obesity following treatment of craniopharyngioma