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Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis

The New England journal of medicine, 1989-07, Vol.321 (1), p.13-16

1989

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Neuropsychiatric Symptoms of Cognitive Impairment and Dementia

1st ed. 2017 edition., 2016

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A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism

The journal of clinical endocrinology and metabolism, 1994-07, Vol.79 (1), p.248-252

1994

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Reference values for height, height velocity and weight in Turner's Syndrome

Acta Paediatrica, 1997-09, Vol.86 (9), p.937-942

1997

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The influence of particles of a minor component on the matrix strength of sodium chloride

European journal of pharmaceutical sciences, 2002-09, Vol.16 (4), p.229-235

2002

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The screening for mutations in the thyroglobulin cDNA from six patients with congenital hypothyroidism

Biochimie, 1999-05, Vol.81 (5), p.425-432

1999

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The role of serum thyroglobulin concentration and thyroid ultrasound imaging in the detection of iodide transport defects in infants

Acta endocrinologica (Copenhagen), 1991-04, Vol.124 (4), p.405-410

1991

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Methionyl human growth hormone in Turner's syndrome

Archives of disease in childhood, 1988-10, Vol.63 (10), p.1211-1217

1988

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Effects of two years of methionyl growth hormone therapy in two dosage regimens in prepubertal children with short stature, subnormal growth rate, and normal growth hormone response to secretagogues

The Journal of pediatrics, 1989-11, Vol.115 (5), p.720-725

1989

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Growth hormone treatment in turner syndrome accelerates growth and skeletal maturation

European journal of pediatrics, 1992-07, Vol.151 (7), p.477-481

1992

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Concentration of plasma thyroglobulin and urinary excretion of iodinated material in the diagnosis of thyroid disorders in congenital hypothyroidism

Acta endocrinologica (Copenhagen), 1983-09, Vol.104 (1), p.27-34

1983

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Prenatal diagnosis of a thyroglobulin synthesis defect in goats

Acta endocrinologica (Copenhagen), 1985-09, Vol.110 (1), p.83-89

1985

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Handbook of Dialogical Self Theory and Psychotherapy: Bridging Psychotherapeutic and Cultural Traditions

1, 2019

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A Controlled Trial of Methionyl Growth Hormone Therapy in Prepubertal Children with Short Stature, Subnormal Growth Rate and Normal Growth Hormone Response to Secretagogues

Acta Paediatrica, 1989-05, Vol.78 (3), p.426-435

1989

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Serum thyroglobulin levels: the physiological decrease in infancy and the absence in athyroidism

The journal of clinical endocrinology and metabolism, 1981-12, Vol.53 (6), p.1301-1303

1981

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2.1 Operating characteristics of a three-dimensional matching and quatitation algorithm for myocardial perfusion studies

Journal of nuclear cardiology, 2001, Vol.8 (1), p.S16-S16

2001

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Iodine-induced hypothyroidism in infants treated with continuous cyclic peritoneal dialysis

The Lancet (British edition), 1990-09, Vol.336 (8718), p.812-812

1990

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The effect of treatment with an LH-RH agonist (Buserelin) on gonadal activity growth and bone maturation in children with central precocious puberty

European journal of pediatrics, 1987-05, Vol.146 (3), p.272-278

1987

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The poikiloderma of Rothmund-Thomson syndrome: changes in Langerhans cell morphology and distribution

Dermatologica, 1989, Vol.179 (4), p.187

1989

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Growth hormone therapy in Turner's syndrome. Impact of injection frequency and initial bone age

American journal of diseases of children (1960), 1992-07, Vol.146 (7), p.817

1992

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A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism

The journal of clinical endocrinology and metabolism, 1994-07, Vol.79 (1), p.248-252

1994

Volltextzugriff (PDF)

Effect of growth hormone administration frequency on 24-hour growth hormone profiles and levels of other growth related parameters in girls with Turner's syndrome

Clinical endocrinology (Oxford), 1993-07, Vol.39 (1), p.77-84

1993

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A Randomized Trial of Intravenous Alteplase before Endovascular Treatment for Stroke

The New England journal of medicine, 2021-11, Vol.385 (20), p.1833-1844

2021

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169 THE ETIOLOGY OF CONGENITAL HYPOTHYROIDISM (CHT) IN THE NETHERLANDS

Pediatric research, 1988-10, Vol.24 (4), p.545-545

1988

Volltextzugriff (PDF)

Growth hormone treatment in Turner syndrome accelerates growth and skeletal maturation. Dutch Growth Hormone Working Group

European journal of pediatrics, 1992-07, Vol.151 (7), p.477-481

1992

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Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis

Neuropsychiatric Symptoms of Cognitive Impairment and Dementia

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism

Reference values for height, height velocity and weight in Turner's Syndrome

The influence of particles of a minor component on the matrix strength of sodium chloride

The screening for mutations in the thyroglobulin cDNA from six patients with congenital hypothyroidism

The role of serum thyroglobulin concentration and thyroid ultrasound imaging in the detection of iodide transport defects in infants

Methionyl human growth hormone in Turner's syndrome

Effects of two years of methionyl growth hormone therapy in two dosage regimens in prepubertal children with short stature, subnormal growth rate, and normal growth hormone response to secretagogues

Growth hormone treatment in turner syndrome accelerates growth and skeletal maturation

Concentration of plasma thyroglobulin and urinary excretion of iodinated material in the diagnosis of thyroid disorders in congenital hypothyroidism

Prenatal diagnosis of a thyroglobulin synthesis defect in goats

Handbook of Dialogical Self Theory and Psychotherapy: Bridging Psychotherapeutic and Cultural Traditions

A Controlled Trial of Methionyl Growth Hormone Therapy in Prepubertal Children with Short Stature, Subnormal Growth Rate and Normal Growth Hormone Response to Secretagogues

Serum thyroglobulin levels: the physiological decrease in infancy and the absence in athyroidism

2.1 Operating characteristics of a three-dimensional matching and quatitation algorithm for myocardial perfusion studies

Iodine-induced hypothyroidism in infants treated with continuous cyclic peritoneal dialysis

The effect of treatment with an LH-RH agonist (Buserelin) on gonadal activity growth and bone maturation in children with central precocious puberty

The poikiloderma of Rothmund-Thomson syndrome: changes in Langerhans cell morphology and distribution

Growth hormone therapy in Turner's syndrome. Impact of injection frequency and initial bone age

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism

Effect of growth hormone administration frequency on 24-hour growth hormone profiles and levels of other growth related parameters in girls with Turner's syndrome

A Randomized Trial of Intravenous Alteplase before Endovascular Treatment for Stroke

169 THE ETIOLOGY OF CONGENITAL HYPOTHYROIDISM (CHT) IN THE NETHERLANDS

Growth hormone treatment in Turner syndrome accelerates growth and skeletal maturation. Dutch Growth Hormone Working Group

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