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Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59 Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
EUROPEAN JOURNAL OF ENDOCRINOLOGY
Effect of growth hormone treatment on hypoglycemia in a patient with both hepatic glycogen synthase and isolated growth hormone deficiencies
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society (Reprinted from J Clin Endocrinol Metab, vol 85, pg 3990-3993,2000)
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Autosomal dominant GH deficiency due to an Arg(183)His GH-1 gene mutation:Clinical and molecular evidence of impaired regulated GH secretion
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade
DIABETOLOGIA
Doping in sport - Preface
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
Growth hormone regulates growth hormone receptor gene transcription in primary human thyroid cells
MOLECULAR AND CELLULAR ENDOCRINOLOGY
Transcription factors in pituitary gland development and their clinical impact on phenotype
HORMONE RESEARCH
Effect of growth hormone and oxandrolone treatment on glucose metabolism in Turner syndrome - A longitudinal study
HORMONE RESEARCH
Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line
JOURNAL OF ENDOCRINOLOGY
Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Regulation of human growth hormone receptor gene transcription by triiodothyronine (T-3)
MOLECULAR AND CELLULAR ENDOCRINOLOGY
Metabolic control in Bernese children and adolescents with diabetes mellitus type I
SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT
What is the value of determining growth hormone-releasing factor (GNRH) inacromegaly?
SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT
"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Aromatase deficiency caused by a novel P450(arom) gene mutation: Impact ofabsent estrogen production on serum gonadotropin concentration in a boy
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Insulin increases serum leptin concentrations in children and adolescents with newly diagnosed Type I diabetes mellitus with and without ketoacidosis
DIABETOLOGIA
MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY
Nature genetics
IDENTIFICATION OF A POTENTIAL TRANSCRIPTION REGULATOR MUTATED IN AUTOIMMUNE POLYGLANDULAR DISEASE-1
European journal of human genetics
CHILDHOOD INSULIN-DEPENDENT DIABETES-MELLITUS - INITIAL PRESENTATION AND MANAGEMENT IN THE 90S
Mineral and electrolyte metabolism
SIMPLE BIOCHEMICAL SCREENING FOR ALDOSTERONE ACTIVITY IN ADRENAL INSUFFICIENCY
European journal of pediatrics
SUPRASELLAR GERMINOMAS IN CHILDHOOD AND ADOLESCENCE - DIAGNOSTIC PITFALLS
Journal of pediatric endocrinology & metabolism
ENDOCRINOLOGY 1997
Schweizerische medizinische Wochenschrift
PREVALENCE OF HUMAN GH-1 GENE ALTERATIONS IN PATIENTS WITH ISOLATED GROWTH-HORMONE DEFICIENCY
Pediatric research
HIGH-FIBER DIETS MAY BE RESPONSIBLE FOR HYPOMAGNESEMIA IN DIABETIC-PATIENTS
Nephron
PHENOTYPIC VARIABILITY IN FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY CAUSED BY A PROP1 GENE MUTATION RESULTING IN THE SUBSTITUTION OF ARG-]CYS AT CODON-120 (R120C)
The Journal of clinical endocrinology and metabolism
INCREASED ENZYMURIA IN DIABETIC CHILDREN WITHOUT PERSISTENT MINIMAL ALBUMINURIA
Nephrology
POSITIONAL CLONING OF THE APECED GENE
Nature genetics
ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS
European journal of endocrinology
EXTRACELLULAR MAGNESIUM DEPLETION IN PEDIATRIC-PATIENTS WITH INSULIN-DEPENDENT DIABETES-MELLITUS
Mineral and electrolyte metabolism
GENETICS OF THE GROWTH-HORMONE AXIS
Journal of pediatric endocrinology & metabolism
REGULATION OF HUMAN GROWTH-HORMONE RECEPTOR GENE-TRANSCRIPTION BY HUMAN GROWTH-HORMONE BINDING-PROTEIN
Molecular and cellular endocrinology
GROWTH PROMOTION AND TURNER-SPECIFIC BONE-AGE AFTER THERAPY WITH GROWTH-HORMONE AND IN COMBINATION WITH OXANDROLONE - WHEN SHOULD THERAPY BE STARTED IN TURNER SYNDROME
Hormone research
EFFECT OF DIFFERENT SERUM CONCENTRATIONS OF GROWTH HORMONE-BINDING PROTEIN (GHBP) ON THE REGULATION OF GH RECEPTOR GHBP GENE-TRANSCRIPTION IN A HUMAN HEPATOMA-CELL LINE/
Hormone research
TREATMENT WITH LOW-DOSE DIAZOXIDE IN 2 GROWTH-RETARDED PREPUBERTAL GIRLS WITH GLYCOGEN-STORAGE-DISEASE TYPE IA RESULTED IN CATCH-UP GROWTH
Journal of inherited metabolic disease
AROMATASE DEFICIENCY IN A FEMALE WHO IS COMPOUND HETEROZYGOTE FOR 2 NEW POINT MUTATIONS IN THE P450(AROM) GENE - IMPACT OF ESTROGENS ON THEHYPERGONADOTROPIC HYPOGONADISM, MULTICYSTIC OVARIES, AND BONE DENSITOMETRY IN CHILDHOOD
The Journal of clinical endocrinology and metabolism
TREATMENT OF FAMILIAL INTRAHEPATIC CHOLESTASIS, DIARRHEA AND GROWTH FAILURE BY CUTANEOUS BILIARY DIVERSION AND INSULIN-LIKE GROWTH-FACTOR-I
Gastroenterology
DIET AND CONTROL OF DIABETES AND WEIGHT I N GIRLS WITH INSULIN-DEPENDENT DIABETES-MELLITUS TYPE-1
Schweizerische medizinische Wochenschrift
GENETIC HOMOGENEITY OF AUTOIMMUNE POLYGLANDULAR DISEASE TYPE-I
American journal of human genetics
GENETICS AND MOLECULAR-BIOLOGY IN SHORT STATURE
Acta paediatrica
MOLECULAR-BIOLOGY AND ITS APPLICATION IN PEDIATRIC ENDOCRINOLOGY
European journal of pediatrics
REGULATION OF HUMAN GROWTH HORMONE-BINDING PROTEIN-PRODUCTION BY HUMAN GROWTH-HORMONE IN A HEPATOMA-CELL LINE
Molecular and cellular endocrinology
ISOLATED GROWTH-HORMONE DEFICIENCY - TESTING THE LITTLE MOUSE HYPOTHESIS IN MAN AND EXCLUSION OF MUTATIONS WITHIN THE EXTRACELLULAR DOMAIN OF THE GROWTH HORMONE-RELEASING HORMONE-RECEPTOR
Pediatric research
BAMHI RFLP FOR THE GHRHR LOCUS
Human molecular genetics
PERSISTENT MICROALBUMINURIA IN ADOLESCENTS WITH TYPE-I (INSULIN-DEPENDENT) DIABETES-MELLITUS IS ASSOCIATED TO EARLY RATHER THAN LATE PUBERTY - RESULTS OF A PROSPECTIVE LONGITUDINAL-STUDY
European journal of pediatrics
IMPACT OF DIFFERENT DOSES OF ETHINYL ESTRADIOL ON REDUCTION OF FINAL HEIGHT IN CONSTITUTIONALLY TALL GIRLS
European journal of pediatrics
HYPERMAGNESIURIA IN CHILDREN WITH NEWLY-DIAGNOSED INSULIN-DEPENDENT DIABETES-MELLITUS
American journal of nephrology
GROWTH-HORMONE CONCENTRATION AND DISAPPEARANCE RATE, INSULIN-LIKE GROWTH-FACTOR-I AND GROWTH-FACTOR-II AND INSULIN LEVELS IN IRON-DEFICIENTVEAL CALVES
Annals of nutrition & metabolism
DIABETES IN CHILDREN AND ADOLESCENTS
Schweizerische medizinische Wochenschrift
HIGH PROXIMAL EXCRETION OF SODIUM DURING ACTIVATION OF BETA-2-ADRENOCRECEPTORS IN HUMANS
Nephron