Results 131 to 140 of about 4,190 (206)

Anomalous origin of right pulmonary artery from ascending aorta (AORPA): An uncommon aortopulmonary vascular anomaly. [PDF]

Lung India
Kaur G, Bhatia A, Menon P, Saxena AK, Sodhi KS.   +4 more
europepmc   +1 more source

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants. [PDF]

Mol Cell Pediatr
Elaraby NM, Metwally AM, Sayed SM, Ashaat NA, Gamal M, Hussen DF, Abuelela S, Ramadan A, Kobesiy MM, Shaker MM, Elgebaly H, Elnady HG, Gammal ME, Ashaat EA.   +13 more
europepmc   +1 more source

Whole Exome Sequencing of a Rare Disease, Mullerian Agenesis and Anorectal Anomaly: A Case Report

Siti Aishah Sulaiman, Nor Azian Abdul Murad, Chow Yock Ping, uhammad-Redha Abdullah-Zawawi, Zam Zureena Mohd Rani, Siti Nurmi Nasir, Salwati Shuib, Dayang Anita Abdul Aziz, Hana Azhari, Sharifah Azween Syed Omar, Zarina Abdul Latiff, Rahman Jamal   +11 more
openalex   +2 more sources

Long-Term Bowel and Urinary Function Outcomes and Quality of Life in Patients with Anorectal Malformations: 20 Years of Experience. [PDF]

Children (Basel)
Baldanza F, Grasso F, Pensabene M, Sergio M, Di Pace MR.   +4 more
europepmc   +1 more source

Neonatal colonic perforation with low anorectal anomaly--(a case report).

, 1989
S Khope, S G Vivekanand
openalex   +1 more source

Urogenital and Other Associated Anomalies in Patients With Anorectal Malformations

, 2011
Mohammad Kazem Sabzehei, Seyed Habibollah Mousavi‐Bahar, Hassan Bazmamoun   +2 more
openalex   +1 more source

Data Sheet 1_Urogenital anomalies in children with anorectal malformations: a single institution observational study.pdf

Belachew Dejene Wondemagegnehu (21171224), Solomon Wubetu Asfaw (21171227)   +1 more
openalex   +1 more source

Adult Presentation of Anorectal Malformation: A 19-Year-Old Woman with a Delayed Diagnosis of Recto-Vestibular Fistula. [PDF]

Am J Case Rep
Bichanga BO, Munyalo FS, Mwende CK, Olwang YA, Okebe S, Lessan J, Mwika PM.   +6 more
europepmc   +1 more source

Prenatal Diagnosis of Fraser Syndrome at 20 Weeks' Gestation: A Case Report and Review of Literature. [PDF]

Cureus
Rana S.
europepmc   +1 more source

Expanding the phenotypic spectrum of Beaulieu-Boycott-Innes syndrome: A case report of a novel THOC6 gene mutation associated with ambiguous genitalia and disorders of sexual development. [PDF]

Medicine (Baltimore)
Humeedat M, Jabareen M, Maraqa B, Sarahneh H, Manasra N.   +4 more
europepmc   +1 more source