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期刊名:Hormone research

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ISSN:0301-0163

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共收录本刊相关文章索引3529
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Henrik B T Christesen,Klaus Brusgaard,Jan Alm et al. Henrik B T Christesen et al.
Background: In severe, medically unresponsive congenital hyperinsulinism (CHI), the histological differentiation of focal versus diffuse disease is vital, since the surgical management is completely different. Genetic ana...
Polyxeni Nicolaidou,Anna Papadopoulou,Y G Matsinos et al. Polyxeni Nicolaidou et al.
Background/aims: Hypocalcemic vitamin D-resistant rickets (HVDRR) is a rare autosomal recessive disorder characterized by severe rickets, hypocalcemia, secondary hyperparathyroidism, elevated levels of 1,25-dihydroxyvitam...
Nancy Unanue,Rodrigo Bazaes,Germán Iñiguez et al. Nancy Unanue et al.
Prader-Willi syndrome (PWS) is a genetic disorder characterized by dysmorphic features, obesity, hypogonadism, hypotonia and mental retardation. Obesity has been linked to insulin resistance and the latter has also been associated with prem...
Sabine E Hannema,Ieuan A Hughes Sabine E Hannema
Wolffian ducts (WDs) are the embryonic structures that form the male internal genitalia. These ducts develop in both the male and female embryo. However, in the female they subsequently regress, whereas in the male they are stabilised by te...
Jakomijn Hoogendam,Hetty Farih-Sips,Ermond van Beek et al. Jakomijn Hoogendam et al.
To gain more insight into the downstream effectors of parathyroid hormone (PTH) related peptide (PTHrP) signaling in chondrocytes, we performed microarray analysis to identify late PTHrP response genes using the chondrogenic ATDC5 cell line...
F P Busse,P Hiermann,A Galler et al. F P Busse et al.
Background: Transferring adolescents with diabetes from pediatric to adult care remains a challenge and the outcome is often unknown. The aims of this study were to determine the patients' perception of transfer arrangeme...
Paolo Ghirri,Christini Ladaki,Ambra Bartoli et al. Paolo Ghirri et al.
Background/aims: Our aim was to investigate glucose homeostasis, insulin sensitivity and insulin-like growth factor (IGF) system status in children born small for gestational age (SGA). ...
Fayza Al-Jenaidi,Outi Makitie,Eyal Grunebaum et al. Fayza Al-Jenaidi et al.
Background: 22q11 deletion syndrome (22q11DS) is characterized by conotruncal cardiac defects and hypoplasia of parathyroid glands and thymus, which result in variable hypoparathyroidism (HPT) and immune deficiency. ...