Results 1 to 10 of about 7,453 (264)

Swyer Syndrome: Clinical Case of Gonadal Dysgenesis in a 15-year-old Girl

open access: yesПедиатрическая фармакология
Swyer syndrome is a rare genetic disorder in which gonadal dysgenesis and karyotype 46, XY are observed. In the postnatal and prepubescent period, this disease has no clinical manifestations and is asymptomatic, which makes diagnosis difficult. The first
Irina V. Karachentsova   +7 more
doaj   +1 more source

Preparing Implementation of Transition Readiness Screening: What Do Paediatric Cancer Survivors and Caregivers Want?

open access: yesChild: Care, Health and Development, Volume 51, Issue 4, July 2025.
ABSTRACT Background Supporting transition from paediatric to adult healthcare is essential for the long‐term well‐being of paediatric cancer survivors. Guided by an implementation science approach, our overall programme of research seeks to integrate transition readiness screening in the routine care of paediatric cancer survivors, using the validated ...
Marika Monarque   +12 more
wiley   +1 more source

The treatment for dysgerminoma of the ovary [PDF]

open access: yesCancer, 1978
Thirty-six patients with pure dysgerminoma of the ovary were treated at the University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute between 1947 and 1974. Twenty-six of these patients had their initial surgery at the M.D. Anderson Hospital or were referred to the M.D.
Felix N. Rutledge   +4 more
openaire   +3 more sources

Lectin‐Histochemical Pattern on the Cystic and Neoplastic Ovaries of Bitches

open access: yesReproduction in Domestic Animals, Volume 60, Issue 5, May 2025.
ABSTRACT Studies have demonstrated that many reproductive disorders can compromise the binding pattern of glycosidic residues, mainly in cows and sows. In the current study, the binding pattern of lectins was characterised and compared in normal and pathological ovaries of bitches.
Juliano P. Terra   +9 more
wiley   +1 more source

Turner Syndrome: Update the Paradigm of Diagnosis, Clinical Care and Consequences of Y cell lines [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2014
Turner’s syndrome (TS) is a common chromosomal aneuploidy, present in humans with an incidence rate of 1:2500 of the new-born infants with phenotypic females.
S Iqbal
doaj   +1 more source

Replenishing co‐downregulated miR‐100‐5p and miR‐125b‐5p in malignant germ cell tumors causes growth inhibition through cell cycle disruption

open access: yesMolecular Oncology, Volume 19, Issue 4, Page 1203-1228, April 2025.
MiR‐99a‐5p/miR‐100‐5p (functionally identical) and miR‐125b‐5p microRNAs are downregulated in malignant germ cell tumors (GCTs). Combination replenishment of these microRNAs using mimics resulted in growth inhibition in representative cell lines, with consequent downregulation of target genes involved in cell cycle (confirmed by flow cytometry) and ...
Marta Ferraresso   +12 more
wiley   +1 more source

Understanding causes of morbidity and mortality in Southern Hemisphere small Odontoceti: a scoping review

open access: yesMammal Review, Volume 55, Issue 2, April 2025.
This review identifies key causes of morbidity and mortality in Southern Hemisphere small Odontoceti, highlighting significant anthropogenic threats and the enhanced need for conservation strategies. Key findings include high rates of entanglements and a diverse range of infectious pathogens. Abstract Marine mammals serve as sentinels for environmental
Rebecca Souter   +3 more
wiley   +1 more source

Nasal immature teratoma in an elderly patient: Clinicopathological and epigenetic analogies with central nervous system counterparts, alongside genomic divergences

open access: yesNeuropathology, Volume 45, Issue 2, Page 100-108, April 2025.
Germ cell tumors (GCTs) are categorized as gonadal or extra‐gonadal, based on the origin. Extra‐gonadal GCTs predominantly manifest within the central nervous system (CNS), mediastinum, retroperitoneum, and sacrococcygeal region. These malignancies are most frequently diagnosed in the pediatric, adolescent, and young adult demographics.
Shintaro Inoue   +15 more
wiley   +1 more source

CTNND1‐Related Disorder: New Insight on Prenatal Phenotype

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 3, March 2025.
ABSTRACT CTNND1 is a gene located in 11q12.1, encoding for p120 catenin, a protein involved in maintaining adherent junctions, regulating the epithelial–mesenchymal transition, and transcriptional signaling of different cellular pathways. Pathogenic variants in CTNND1 are classically associated with isolated cleft palate and Blefaro‐cheilo‐dontic ...
B. Conti   +12 more
wiley   +1 more source

Dysgerminoma of the Left Ovary in a Patient with Balanced Translocation 46X, t(X:1) (q22;q21): A Case Report

open access: yesInternational Medical Case Reports Journal, 2023
Koh Nagata, Takako Shimada, Chiaki Eishi, Masaki Nishi, Toru Murakami, Kazuaki Ohashi, Itsuki Kajimura, Kiyonori Miura Obstetrics and Gynecology, Nagasaki University Hospital, Nagasaki, JapanCorrespondence: Koh Nagata, Obstetrics and Gynecology, Nagasaki
Nagata K   +7 more
doaj  

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