Results 261 to 270 of about 85,956 (353)

Risk factors for glucocorticoid induced osteoporosis in young adults. [PDF]

open access: yesFront Endocrinol (Lausanne)
Florez H   +10 more
europepmc   +1 more source

Next Generation Sequencing Allows Identification of a Novel Mutation in the TfR2 Gene and Outperforms the Conventional Diagnostic Techniques

open access: yeseJHaem, Volume 6, Issue 4, August 2025.
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]

open access: yesLife (Basel)
Asgeirsson A   +11 more
europepmc   +1 more source

Intramuscular injection of testosterone undecanoate for the treatment of male hypogonadism: phase I studies

open access: bronze, 1999
H. M. Behre   +4 more
openalex   +1 more source

The Role of Ferroptosis in Women's Health and Diseases

open access: yesMedComm, Volume 6, Issue 8, August 2025.
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

Endocrine Abnormalities and Growth Pattern in Single Large‐Scale Mitochondrial DNA Deletion Syndromes

open access: yesActa Paediatrica, Volume 114, Issue 8, Page 1857-1867, August 2025.
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

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