Results 141 to 150 of about 129,423 (272)
Abstract Background In juvenile granulosa cell tumors (juvGCTs), impaired survival was reported after preoperative tumor rupture, peritoneal metastases, or high mitotic rate (≥20 mitoses per 10 high‐power fields). Therefore, a risk stratification was developed to select patients for chemotherapy. Methods Between 2001 and 2019, 89 female patients and 24
Dominik T. Schneider+12 more
wiley +1 more source
Primary Amenorrhea and Differences of Sex Development. [PDF]
Naroji S, Gomez-Lobo V, Finlayson C.
europepmc +1 more source
Managing pregnancy with long‐term parenteral nutrition: A case report and review of the literature
Abstract Parenteral nutrition (PN) is essential for patients with chronic intestinal failure but poses significant challenges during pregnancy because of increased nutrition needs and associated risks such as central line–associated bloodstream infections. We report a case of a 29‐year‐old primigravid woman with Crohn's disease who required chronic PN.
Muhammad Shahzil+6 more
wiley +1 more source
Primary Amenorrhea with Apparently Absent Uterus: A Report of Three Cases. [PDF]
Porsius E+4 more
europepmc +1 more source
Primary Amenorrhea Accompanied by Adrenal Adenoma: Start of Menarche Soon after Tumor Resection.
Yoshimi Takahashi+13 more
openalex +2 more sources
Tissue Engineering and Regenerative Medicine: Perspectives and Challenges
Tissue engineering and regenerative medicine. This review presents cell therapy, extracellular vesicle therapy, and tissue engineering in regenerative medicine, highlighting their key historical milestones, clinical applications, and current challenges.
Van T. Hoang+12 more
wiley +1 more source
ABSTRACT Background Autosomal recessive severe congenital neutropenia (SCN) has been associated with homozygous variants in the HAX1 gene. The aim of this cross‐sectional study was to evaluate the gonadal function and pubertal development in pediatric patients with SCN due to HAX1 gene variant (HAX1‐SCN).
Deniz Özalp Kızılay+20 more
wiley +1 more source
A rare case of Swyer syndrome from Pakistan in a young girl with primary amenorrhea and 46XY genotype. [PDF]
Jawed I+5 more
europepmc +1 more source