Published in Diabetes Care on March 01, 2007
The meter of metabolism. Cell (2008) 5.71
Circadian rhythms and metabolic syndrome: from experimental genetics to human disease. Circ Res (2010) 2.49
Guidelines for optimal bolus calculator settings in adults. J Diabetes Sci Technol (2011) 1.37
The REV-ERBs and RORs: molecular links between circadian rhythms and lipid homeostasis. Future Med Chem (2011) 1.08
The use of insulin pumps in youth with type 1 diabetes. Diabetes Technol Ther (2010) 0.91
Changes in Insulin Requirements From the Onset of Continuous Subcutaneous Insulin Infusion (CSII) Until Optimization of Glycemic Control. J Diabetes Sci Technol (2014) 0.90
Predicting the optimal basal insulin infusion pattern in children and adolescents on insulin pumps. Diabetes Care (2013) 0.79
Impact of ELKa, the Electronic Device for Prandial Insulin Dose Calculation, on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus: A Randomized Controlled Trial. J Diabetes Res (2017) 0.75
Polymorphic basal rates of continuous subcutaneous insulin infusion among Taiwanese children with type 1 diabetes. Biomed Res Int (2015) 0.75
Frequency of SMBG correlates with HbA1c and acute complications in children and adolescents with type 1 diabetes. Pediatr Diabetes (2011) 3.16
Epidemiology and initial management of ambiguous genitalia at birth in Germany. Horm Res (2006) 2.02
Novel associations in disorders of sex development: findings from the I-DSD Registry. J Clin Endocrinol Metab (2013) 1.76
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance. J Clin Endocrinol Metab (2012) 1.68
Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy. J Clin Endocrinol Metab (2007) 1.41
Abnormalities in emotion processing within cortical and subcortical regions in criminal psychopaths: evidence from a functional magnetic resonance imaging study using pictures with emotional content. Biol Psychiatry (2003) 1.40
Deletion and point mutations of PTHLH cause brachydactyly type E. Am J Hum Genet (2010) 1.35
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiency. Eur J Endocrinol (2009) 1.23
Co-localisation of the Kir6.2/SUR1 channel complex with glucagon-like peptide-1 and glucose-dependent insulinotrophic polypeptide expression in human ileal cells and implications for glycaemic control in new onset type 1 diabetes. Eur J Endocrinol (2007) 1.23
Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype. Diabetes Care (2011) 1.19
Basal rates and circadian profiles in continuous subcutaneous insulin infusion (CSII) differ for preschool children, prepubertal children, adolescents and young adults. Pediatr Diabetes (2011) 1.18
Difficulties in diagnosis and treatment of 5alpha-reductase type 2 deficiency in a newborn with 46,XY DSD. Horm Res Paediatr (2010) 1.13
Cardiovascular risk in 26,008 European overweight children as established by a multicenter database. Obesity (Silver Spring) (2008) 1.13
Type 2 diabetes in children and adolescents in a 2-year follow-up: insufficient adherence to diabetes centers. Horm Res (2007) 1.11
Reduced prevalence of diabetic ketoacidosis at diagnosis of type 1 diabetes in young children participating in longitudinal follow-up. Diabetes Care (2011) 1.11
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapy. Eur J Pediatr (2008) 1.04
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study. J Clin Endocrinol Metab (2011) 1.03
Health-related quality of life in overweight and obese youths: results of a multicenter study. Health Qual Life Outcomes (2010) 1.02
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus. J Bone Miner Res (2011) 1.01
PCR-based analysis of differentially methylated regions of GNAS enables convenient diagnostic testing of pseudohypoparathyroidism type Ib. Clin Chem (2008) 0.96
Glucose metabolism and neurological outcome in congenital hyperinsulinism. Semin Pediatr Surg (2011) 0.95
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene. Eur J Endocrinol (2005) 0.93
Current use of metformin in addition to insulin in pediatric patients with type 1 diabetes mellitus: an analysis based on a large diabetes registry in Germany and Austria. Pediatr Diabetes (2014) 0.93
Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription. J Mol Med (Berl) (2006) 0.93
Differential gene-expression patterns in genital fibroblasts of normal males and 46,XY females with androgen insensitivity syndrome: evidence for early programming involving the androgen receptor. Genome Biol (2003) 0.92
Androgen insensitivity syndrome. Semin Reprod Med (2012) 0.90
Psychosexual development in adolescents and adults with disorders of sex development--results from the German Clinical Evaluation Study. J Sex Med (2012) 0.90
Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development. Eur J Endocrinol (2012) 0.89
Gender role behavior in children with XY karyotype and disorders of sex development. Horm Behav (2007) 0.88
Deciding on gender in children with intersex conditions: considerations and controversies. Treat Endocrinol (2005) 0.88
Medical and psychosocial implications of adolescent extreme obesity - acceptance and effects of structured care, short: Youth with Extreme Obesity Study (YES). BMC Public Health (2013) 0.88
Association of parvovirus B19 infection and Hashimoto's thyroiditis in children. Viral Immunol (2008) 0.87
Patients with disorders of sex development (DSD) at risk of gonadal tumour development: management based on laparoscopic biopsy and molecular diagnosis. BJU Int (2012) 0.85
The A645D mutation in the hinge region of the human androgen receptor (AR) gene modulates AR activity, depending on the context of the polymorphic glutamine and glycine repeats. J Clin Endocrinol Metab (2006) 0.85
Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor. J Bone Miner Res (2011) 0.84
Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome. BMC Genomics (2007) 0.83
A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones. J Pediatr Endocrinol Metab (2011) 0.83
Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome. J Mol Med (Berl) (2009) 0.83
Health-related quality of life in children with disorders of sex development (DSD). Eur J Pediatr (2014) 0.83
Association of epilepsy and type 1 diabetes mellitus in children and adolescents: is there an increased risk for diabetic ketoacidosis? J Pediatr (2011) 0.82
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency. J Clin Endocrinol Metab (2007) 0.82
Long-term follow-up of bone mineral density in childhood hypophosphatasia. Joint Bone Spine (2007) 0.82
Determination of Gs alpha protein activity in Albright's hereditary osteodystrophy. J Pediatr Endocrinol Metab (2006) 0.82
Minor hypospadias: the "tip of the iceberg" of the partial androgen insensitivity syndrome. PLoS One (2013) 0.81
17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17betaHSD3 gene. J Pediatr Endocrinol Metab (2012) 0.81
Disorders of sex development expose transcriptional autonomy of genetic sex and androgen-programmed hormonal sex in human blood leukocytes. BMC Genomics (2009) 0.80
Parental preference of prandial insulin aspart compared with preprandial human insulin in a basal-bolus scheme with NPH insulin in a 12-wk crossover study of preschool children with type 1 diabetes. Pediatr Diabetes (2007) 0.80
P450 side-chain cleavage deficiency--a rare cause of congenital adrenal hyperplasia. Endocr Dev (2010) 0.80
Sinorhizobium meliloti CheA complexed with CheS exhibits enhanced binding to CheY1, resulting in accelerated CheY1 dephosphorylation. J Bacteriol (2011) 0.80
Isoenzyme type 1 of 5alpha-reductase is abundantly transcribed in normal human genital skin fibroblasts and may play an important role in masculinization of 5alpha-reductase type 2 deficient males. Eur J Endocrinol (2005) 0.80
Boy with pseudohypoparathyroidism type 1a caused by GNAS gene mutation (deltaN377), Crouzon-like craniosynostosis, and severe trauma-induced bleeding. Am J Med Genet A (2009) 0.80
We used to call them hermaphrodites. Genet Med (2007) 0.79
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interaction. J Clin Endocrinol Metab (2008) 0.79
Predicting the optimal basal insulin infusion pattern in children and adolescents on insulin pumps. Diabetes Care (2013) 0.79
A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy. Eur J Endocrinol (2003) 0.79
Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5. J Clin Res Pediatr Endocrinol (2010) 0.79
Different pattern of epigenetic changes of the GNAS gene locus in patients with pseudohypoparathyroidism type Ic confirm the heterogeneity of underlying pathomechanisms in this subgroup of pseudohypoparathyroidism and the demand for a new classification of GNAS-related disorders. J Clin Endocrinol Metab (2014) 0.79
Androgen receptor function links human sexual dimorphism to DNA methylation. PLoS One (2013) 0.79
46,XY disorders of sex development--the undermasculinised male with disorders of androgen action. Best Pract Res Clin Endocrinol Metab (2010) 0.79
Parent and health professional perspectives in the management of adolescents with diabetes: development of assessment instruments for international studies. Qual Life Res (2006) 0.79
Tracking and prediction of arterial blood pressure from childhood to young adulthood in 868 patients with type 1 diabetes: a multicenter longitudinal survey in Germany and Austria. Diabetes Care (2008) 0.78
46,XY disorder of sex development in a sudanese patient caused by a novel mutation in the HSD17B3 gene. Sex Dev (2014) 0.78
Utilization of health care services and satisfaction with care in adults affected by disorders of sex development (DSD). J Gen Intern Med (2014) 0.78
Characteristic features of reproductive hormone profiles in late adolescent and adult females with complete androgen insensitivity syndrome. Sex Dev (2015) 0.77
17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal. Gynecol Endocrinol (2006) 0.77
"Any decision is better than none" decision-making about sex of rearing for siblings with 17beta-hydroxysteroid-dehydrogenase-3 deficiency. Arch Sex Behav (2006) 0.77
Pulse pressure in children and adolescents with type 1 diabetes mellitus in Germany and Austria. Pediatr Diabetes (2014) 0.77
Understanding differences and disorders of sex development. Foreword. Endocr Dev (2014) 0.77
46,XY karyotype in a female phenotype fetus: a challenging diagnosis. J Pediatr Adolesc Gynecol (2012) 0.76
Molecular Diagnosis of Multiple Endocrine Neoplasia (MEN) in Paraffin-Embedded Specimens. Endocr Pathol (1995) 0.76
Steroid 5alpha-reductase 1 polymorphisms and testosterone/dihydrotestosterone ratio in male patients with hypospadias. Horm Res (2004) 0.76
Sensitivity analysis of weight reduction results of an observational cohort study in overweight and obese children and adolescents in Germany: the evakuj study. Pediatr Rep (2013) 0.75
Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene. J Clin Res Pediatr Endocrinol (2016) 0.75
Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene. J Clin Res Pediatr Endocrinol (2015) 0.75
Disorders of sex development and hypogonadism: genetics, mechanism, and therapies. Int J Endocrinol (2012) 0.75
Hormonal management of complete androgen insensitivity syndrome from adolescence onward. Horm Res Paediatr (2011) 0.75
The First Egyptian-German workshop on disorders of sex development (DSD) National Research Centre, Cairo, Egypt, 24-25 November 2007. Pediatr Endocrinol Rev (2008) 0.75
Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs. J Steroid Biochem Mol Biol (2006) 0.75
Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency . Horm Res Paediatr (2016) 0.75
Initial insulin therapy in children and adolescents with type 1 diabetes mellitus. Pediatr Diabetes (2009) 0.75
Intersex - from gene to gender. Lubeck, Germany, 1-3 April 2004. Pediatr Endocrinol Rev (2004) 0.75
A novel missense mutation of 5-alpha reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish family. Urology (2005) 0.75
Gonadectomy in Complete Androgen Insensitivity Syndrome: Why and When? Sex Dev (2017) 0.75
[Intersexual children. Who decides on their sex?]. MMW Fortschr Med (2004) 0.75
A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation. Clin Dysmorphol (2010) 0.75
Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome. Sex Dev (2017) 0.75
Uniparental Disomy in Somatic Mosaicism 45,X/46,XY/46,XX Associated with Ambiguous Genitalia. Sex Dev (2015) 0.75
Effect of GH replacement therapy in two male siblings with combined X-linked hypophosphatemia and partial GH deficiency. Eur J Endocrinol (2003) 0.75
First diagnosis of Martin-Albright syndrome in a 58-year-old patient. J Dtsch Dermatol Ges (2009) 0.75
Preserved fertility in a patient with gynecomastia associated with the p.Pro695Ser mutation in the androgen receptor. Sex Dev (2014) 0.75
Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene Mutation. Sex Dev (2015) 0.75
[Acute kidney injury in liver failure]. Dtsch Med Wochenschr (2016) 0.75
RWDD1 interacts with the ligand binding domain of the androgen receptor and acts as a coactivator of androgen-dependent transactivation. Mol Cell Endocrinol (2012) 0.75
[Incomplete androgen insensitivity]. Orv Hetil (2006) 0.75
Disorders of sex development (DSD). Preface. Sex Dev (2010) 0.75
Pseudohypoparathyroidism type IA (PHP-Ia): maternally inherited GNAS gene mutation. J Pediatr Endocrinol Metab (2009) 0.75
Three out of four: a case discussion on ambiguous genitalia. Eur J Endocrinol (2008) 0.75
Mutational analysis of Hungarian patients with androgen insensitivity syndrome. J Pediatr Endocrinol Metab (2003) 0.75