Results 261 to 270 of about 85,956 (353)
Risk factors for glucocorticoid induced osteoporosis in young adults. [PDF]
Florez H+10 more
europepmc +1 more source
Male Hypogonadism Caused by Homozygous Deletion of Exon 10 of the Luteinizing Hormone (LH) Receptor: Differential Action of Human Chorionic Gonadotropin and LH [PDF]
Jörg Gromoll+3 more
openalex +1 more source
ABSTRACT Introduction Type 3 hereditary hemochromatosis (HH) is a rare genetic disease due to mutations in the transferrin receptor 2 (TFR2) gene. Methods and Results Here, we describe the case of an Italian patient presenting with hyperferritinemia and hepatic iron accumulation, not evidenced by magnetic resonance imaging, that was subsequently ...
Miriam Longo+9 more
wiley +1 more source
Spontaneous Improvement of Hypogonadotropic Hypogonadism in a Patient with <i>PCSK1</i> and <i>HS6ST1</i> Mutations: A Case Report. [PDF]
Asgeirsson A+11 more
europepmc +1 more source
The Role of Ferroptosis in Women's Health and Diseases
At present, there are many common women's diseases, such as preeclampsia (PE), ovarian cancer, and cervical cancer, endangering women's health. These diseases all over the world are characterized by high morbidity and mortality. In the past decade, ferroptosis, a unique pattern of programmed cell death primarily driven by iron‐dependent phospholipid ...
Qiang Xu+5 more
wiley +1 more source
<i>SOX2</i> Variant Resulting in Hypogonadotropic Hypogonadism, Learning Difficulties, and Ear (Rather Than Eye) Anomalies. [PDF]
Cher WQ, Chan D.
europepmc +1 more source
The low responder, hypogonadotropic hypogonadism female patient in IVF: do not give up! [PDF]
Nathan Lewit, Shahar Kol
openalex +1 more source
ABSTRACT Aim To assess the prevalence of endocrine disorders and investigate growth patterns in single large‐scale mitochondrial DNA deletion syndromes (SLSMDs). Methods A retrospective study of all children with SLSMD who attended Sheba Medical Center, Israel, from February 2017 to September 2024.
Ayman Daka+7 more
wiley +1 more source