• A 10-year retrospective study of the risks and peculiarities in pediatric patients with (para)gonadal tumors and cysts
• A Case of Dysgerminoma in a Pediatric Patient with a PIK3CD Mutation
• A Comprehensive Review of Current Trends in the Diagnosis and Treatment of Ovarian Germ Cell Tumors
• A non-pregnant woman with elevated beta-HCG: A rare case of ovarian seminoma
• A Perplexing Case of a Germ Cell Tumor: A Case Report
• A rare case of ovarian gonadoblastoma flourishing into malignant mixed germ cell tumour with review of literature
• A rare case of Swyer syndrome from Pakistan in a young girl with primary amenorrhea and 46XY genotype
• A RETROSPECTIVE STUDY OF DISEASE PROCESSES IN MANED WOLVES (<em>CHRYSOCYON BRACHYURUS</em>) IN NORTH AMERICAN ZOOLOGICAL INSTITUTIONS WITH EMPHASIS ON UROLITHIASIS, INFLAMMATORY BOWEL DISEASE, AND NEOPLASIA
• Adult ovarian and sellar region mixed germ cell tumor: a case report and literature review
• Assessment of Molecular Markers in Pediatric Ovarian Tumors: Romanian Single-Center Experience
• AZFa candidate gene <em>UTY</em> and its X homologue <em>UTX</em> are expressed in human germ cells
• Bilateral Gonadal Dysgerminoma in a Phenotypic Female With 46,XY Disorder of Sexual Development: A Case Report
• Bilateral Gonadoblastoma Overgrown by Dysgerminoma of the Right Gonad in a Patient with Swyer Syndrome
• Cancer Stem Cell Markers Are Differentially Expressed in Malignant Ovarian Germ Cell Tumors
• Case Report: From epilepsy and uterus didelphys to Turner syndrome-associated dysgerminoma
• Challenges in the management of Turner syndrome with Y chromosome material: a case report of prophylactic gonadectomy revealing dysgerminoma
• Challenging gestational trophoblastic disease cases and mimics: An exemplar for the management of rare tumours
• Chylous ascites following retroperitoneal lymphadenectomy in a patient with recurrent dysgerminoma of ovary: A case report
• Clinical and ultrasonographic findings of ovarian tumours in bitches: A retrospective study
• Clinical Challenges in the Management of Malignant Ovarian Germ Cell Tumours
• Clinical Characterization of Patients with Ovarian Mass Combined with Dysplasia of Secondary Sexual Characteristics
• Comparison of overall and patterns of care in patients with a malignant ovarian germ cell tumor by age in the United States: a National Cancer Database (2004-2016) analysis
• Complete gonadal dysgenesis analysis in the population of Latvia: malignant outcomes and a review of literature
• Component Patterns and Survival Outcomes in Patients with Mixed Malignant Ovarian Germ Cell Tumors: A Retrospective Cohort Study
• Comprehensive microRNA expression analysis of pediatric gonadal germ cell tumors: unveiling novel biomarkers and signatures
• Conservative surgical staging as a means to preserve fertility in patients with dysgerminoma: a case report
• Controlled ovarian stimulation in cancer patients under 18 years old; a case series
• Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice
• Diagnosis and Management of Dysgerminomas with a Brief Summary of Primitive Germ Cell Tumors
• Diagnostically misleading aberrant terminal deoxynucleotidyl transferase expression in germ cell tumors
• Diffusion-weighted imaging in pediatric extracranial germ cell tumors
• Dissecting Gonadoblastoma of the Ovary Coexistent with an Atypical Endometriotic Cyst: Incidental Detection in Cystectomy Specimen of a Woman with 46,XX Karyotype
• Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report
• Dysgerminoma Masquerading as Gestational Trophoblastic Neoplasia
• Dysgerminoma of the Left Ovary in a Patient with Balanced Translocation 46X, t(X:1) (q22;q21): A Case Report
• Dysgerminoma of the ovary
• Dysgerminoma Probably Due to a Novel SOHLH1-pathogenic Variant Causing Familial Ovarian Dysgenesis
• Elevated lactate dehydrogenase - A red herring in the diagnosis of a sclerosing stromal tumor: A case report
• Epidemiological profile and clinico-pathological features of pediatric gynecological cancers at Moi Teaching &amp; Referral Hospital, Kenya
• Expression of p16 Tumor Suppressor Protein in Malignant Ovarian Germ Cell Tumors; Immunohistochemical Study
• Extraovarian Dysgerminoma Involving the Uterine Cervix: A Rare Case Report With Literature Review
• Fertility-sparing approach to malignant ovarian germ cell tumors - Oncologic and obstetric outocome: A retrospective study
• Frequent expression of CD45RO memory T cell marker as well as low to high expression of PD-1 and PD-L1 inhibitory molecules in seminoma and dysgerminoma
• Genetic characteristics of ovarian malignant germ cell tumors
• Germ Cell Tumors of the Ovary: A Review
• Giant ovarian dysgerminoma in adolescent: A case report
• Giant ovarian dysgerminoma in an adolescent
• Gonadal tumor development in 46,XX disorders of gonadal development
• Gonadal tumor risk in pediatric and adolescent phenotypic females with disorders of sex development and Y chromosomal constitution with different genetic etiologies
• Gonadoblastoma with Dysgerminoma Presenting as Virilizing Disorder in a Young Child with 46, XX Karyotype: A Case Report and Review of the Literature
• Gonadoblastoma: Clinicopathological study and literature review of 3 cases
• Imaging appearance of ovarian dysgerminoma: A report of two cases
• Immature Teratoma: Diagnosis and Management-A Review of the Literature
• Impact of Optimal Therapy and Prognostic Factors in Malignant Germ Cell Tumors of Ovary: 20 Years' Institutional Experience
• Late Diagnosis of Swyer Syndrome in a Patient with Bilateral Germ Cell Tumor Treated with a Contraceptive Due to Primary Amenorrhea
• Late presentation of Swyer syndrome: A case report
• Malignant Germ Cell Tumors of the Ovary: Clinical and Imaging Features
• Malignant ovarian and testicular germ cell tumors: Common characteristics but different prognoses
• Malignant ovarian dysgerminoma in a 16-year-old leopard gecko (<em>Eublepharis macularius</em>)
• Malignant ovarian dysgerminoma in a 16-year-old leopard gecko (Eublepharis macularius)
• Metachronous bilateral ovarian tumors: Immature teratoma and dysgerminoma
• Metastasis of ovarian dysgerminoma in a postmenopausal patient: a rare case report
• Metastatic germ cell tumour in effusion cytology
• MR Imaging of Germ Cell and Sex Cord Stromal Tumors
• Non-obvious diagnosis and breast development in pure gonadal dysgenesis
• Oncology and reproductive outcomes over 16 years of malignant ovarian germ cell tumors treated by fertility sparing surgery
• Ovarian cancer during pregnancy
• Ovarian dysgerminoma
• Ovarian Dysgerminoma - Challenging Presurgical Diagnosis and Mini-Mally Invasive Treatment
• Ovarian dysgerminoma: clues to the radiological diagnosis
• Ovarian Germ Cell Tumors in North-Western India: A Comprehensive 3-Year Retrospective Study of 145 Cases at a Tertiary Cancer Hospital
• Ovarian gonadoblastoma with dysgerminoma in a girl with 46,XX karyotype 17a-hydroxylase/17, 20-lyase deficiency: A case report and literature review
• Ovarian Masses in Children and Adolescents: A Review of the Literature with Emphasis on the Diagnostic Approach
• Paediatric Ovarian Dysgerminoma: A Case Report
• Paraneoplastic neuromyelitis optica spectrum disorder associated with ovarian dysgerminoma: a case report and literature review
• Pediatric pseudo-Meigs syndrome with ovarian dysgerminoma
• Predicting outcomes in female germ cell tumors using a modified International Germ Cell Cancer Collaborative Group classification system to guide management
• Prevalence, distribution, and risk markers for the development of gonadal germ cell tumors in patients with certain types of disorders of sexual differentiation with Y chromosome - A retrospective study
• Primary Dysgerminoma of the Uterine Cervix: A Rare Case Report
• Primary Mediastinal Dysgerminoma: A Case Report and Literature Review
• Primary ovarian lymphoma: A case report
• Primary ovarian tumors in children: a single center experience of 124 patients
• Pure 46, XY gonadal dysgenesis and 46, XY complete androgen insensitivity syndrome: A case report
• Pure ovarian dysgerminoma in a postmenopausal patient: A case report and review of the management
• Rare Case of a Turner Syndrome Patient with Metastatic Dysgerminoma and No Y-Chromosomal Material with Pathogenic Variants Found in KIT and MTOR
• Rare case of Turner syndrome patient with metastatic dysgerminoma and no Y-chromosomal material with pathogenic variants found in KIT and MTOR
• Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation
• Review of neoplasia in fish at a large display aquarium, 2005-2021
• Revisiting Surgery in the Current Era of Gamma Knife for Cavernous Sinus Lesions
• Seminoma and dysgerminoma: evidence for alignment of clinical trials and de-escalation of systemic chemotherapy
• Spectrum of Germ Cell Tumor (GCT): 5 Years' Experience in a Tertiary Care Center and Utility of OCT4 as a Diagnostic Adjunct
• Spontaneous pregnancy after fertility-sparing surgery and adjuvant chemotherapy for advanced pure dysgerminoma: A case report
• Spontaneous Tumor Lysis Syndrome in a Young Girl with Dysgerminoma: A Case Report
• SRY-positive 45,X/46,XY karyotype in a phenotypically Turner-like Chinese adolescent female with ovarian dysgerminoma and gonadoblastoma
• Study of neoadjuvant chemotherapy in advanced malignant ovarian germ cell tumors at a tertiary center in western India
• Surgical management and outcomes for stage 1 malignant ovarian germ cell tumours: A UK multicentre retrospective cohort study
• Swyer Syndrome Presenting as Dysgerminoma: A Case Report
• Swyer syndrome with gonadal non-dysgerminoma malignant germ cell tumors: a report of 15 cases in a national medical center
• Undetectable anti-Mullerian hormone and inhibin B do not preclude the presence of germ cell tumours in 45,X/46,XY or 46,XY gonadal dysgenesis
• Yolk sac tumor and dysgerminoma in the left gonad following gonadoblastoma in the right gonad in a 46,XY DSD with a novel SRY missense mutation: a case report