Results 11 to 20 of about 3,123,862 (240)

Vaginoplasty for disorders of sex development [PDF]

open access: yesFrontiers in Endocrinology, 2013
One of the most common problem found in patients with Disorders of Sexual Developments (DSD) is the absence or extreme hypoplasia of the vagina. The type of patients presenting this anomaly may belong to complete different groups: - patients with a ...
Giacinto A. Marrocco   +6 more
doaj   +3 more sources

Ultrasonography for disorders of sex development in pediatrics [PDF]

open access: yesFrontiers in Pediatrics
ObjectiveThis study aimed to evaluate the clinical value of ultrasonography in the management of disorders of sex development (DSDs).MethodsUltrasonographic appearance and clinical data of 82 cases with DSD were reviewed retrospectively.ResultsIn total ...
Yuting Wu   +3 more
doaj   +2 more sources

Current Diagnostic Approaches in the Genetic Diagnosis of Disorders of Sex Development [PDF]

open access: yesJCRPE
Disorders of sex development (DSD) are a clinically and genetically highly heterogeneous group of congenital disorders. The most accurate and rapid diagnosis may be possible with a complementary multidisciplinary diagnostic approach, including ...
Deniz Özalp Kızılay, Samim Özen
doaj   +2 more sources

Ovotesticular disorders of sex development with dysgerminoma in a 46, XX/46, XY female: A case report [PDF]

open access: yesGynecologic Oncology Reports
The diagnosis of ovotesticular disorders of sex development can only be confirmed when both testicular and ovarian tissues are present simultaneously in the same individual, regardless of the patient’s karyotype. This report aims to discuss the diagnosis
Yafei Xue   +4 more
doaj   +2 more sources

Editorial: Shared decision making in pediatric differences/disorders of sex development [PDF]

open access: yesFrontiers in Urology, 2023
Kristina Suorsa-Johnson   +5 more
doaj   +2 more sources

Disorders of Sex Development [PDF]

open access: yesKorean Journal of Urology, 2012
The birth of a new baby is one of the most dramatic events in a family, and the first question is usually "is it a boy or a girl?" The newborn infant with ambiguous external genitalia often comes as a surprise for the doctors as well as the parents and is sometimes described as an endocrine emergency situation presenting a problem of sex assignment ...
Kun Suk Kim, Jongwon Kim
  +8 more sources

Disorders of Sex Development

open access: yesPediatrics In Review, 2021
1. Alejandro Diaz, MD*,† 2. Elizabeth G. Lipman Diaz, PhD, ARNP, CPNP‡ 1. *Nicklaus Children’s Hospital, Miami, FL 2. †Herbert Wertheim College of Medicine, Florida International University, Miami, FL 3. ‡University of Miami School of Nursing and Health Studies, Coral Gables, FL * Abbreviations: AMH: : anti-mullerian hormone
Alejandro Diaz   +2 more
openaire   +5 more sources

Multiple sclerosis clinical decision support system based on projection to reference datasets

open access: yesAnnals of Clinical and Translational Neurology, Volume 9, Issue 12, Page 1863-1873, December 2022., 2022
Abstract Objective Multiple sclerosis (MS) is a multifactorial disease with increasingly complicated management. Our objective is to use on‐demand computational power to address the challenges of dynamically managing MS. Methods A phase 3 clinical trial data (NCT00906399) were used to contextualize the medication efficacy of peg‐interferon beta‐1a vs ...
Chadia Ed‐driouch   +13 more
wiley   +1 more source

Phenotypic continuum of NFU1‐related disorders

open access: yesAnnals of Clinical and Translational Neurology, Volume 9, Issue 12, Page 2025-2035, December 2022., 2022
Abstract Bi‐allelic variants in Iron–Sulfur Cluster Scaffold (NFU1) have previously been associated with multiple mitochondrial dysfunctions syndrome 1 (MMDS1) characterized by early‐onset rapidly fatal leukoencephalopathy. We report 19 affected individuals from 10 independent families with ultra‐rare bi‐allelic NFU1 missense variants associated with a
Rauan Kaiyrzhanov   +45 more
wiley   +1 more source

A potential biomarker of cognitive impairment: The olfactory dysfunction and its genes expression

open access: yesAnnals of Clinical and Translational Neurology, Volume 9, Issue 12, Page 1884-1897, December 2022., 2022
Abstract Objective Accumulation evidence has reported that olfactory impairment may be an essential clinical marker and predictor of mild cognitive impairment or Alzheimer's disease. Method Participants were enrolled in the population‐based, prospective study in Fuxin county, Liaoning province, China between 2019 and 2021.
Jiayi Song   +11 more
wiley   +1 more source

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