Results 51 to 60 of about 341 (88)

Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated asplenia. [PDF]

Mol Cytogenet, 2021
Oszer A, Bąbol-Pokora K, Kołtan S, Pastorczak A, Młynarski W.   +4 more
europepmc   +1 more source

SDF2 and SDF2L1 are essential co-factors of DNAJB11 for Polycystin-1 processing. [PDF]

J Biol Chem
Busch T, Neubauer B, Sediq S, Zeisler PC, Tholen S, Schilling O, Westermann L, Köttgen M.   +7 more
europepmc   +1 more source

Fetal MRI: abdominal cystic lesions. [PDF]

Insights Imaging
Castellanos DG, Rodríguez MR, Greciano LS, Del Hoyo AA, Moreno AD, Alcolea JL, Sampietro C, de Vega VM.   +7 more
europepmc   +1 more source

Lateral Heterotaxy Syndrome in a Newborn Caucasian Male. [PDF]

Cureus, 2020
Koenig ZA, Verhoeven A, Rosen D, Petrone AB.   +3 more
europepmc   +1 more source

Heterotaxy Syndrome With Right Isomerism and Interrupted Inferior Vena Cava: A Case Report and Literature Review. [PDF]

Cureus
Iskafi RA, Abugharbieh Y, Ahmad I, Shweki H, Dwaik HA.   +4 more
europepmc   +1 more source

Laparoendoscopic Single-Site Surgery (LESS) for Right Donor Nephrectomy in a Patient With Situs Inverses Totalis: A Novel Approach for Such a Case. [PDF]

Cureus
Almalki AM, Fikri J, Jouhar TM, Khalaf A, Aboalsamh GA.   +4 more
europepmc   +1 more source

Renal cell carcinoma in an adult-onset ESRD patient with nephronophthisis harboring NPHP3 deletion: A case report. [PDF]

Heliyon
Li ZL, Wang FM, Wen Y, Ni HF, Zhang XL, Wang B.   +5 more
europepmc   +1 more source

Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis. [PDF]

Eur J Case Rep Intern Med, 2020
Dinis-Ferreira S, Lemos C, Caldeira M, Homem-Costa M, da Luz Brazão M, Aveiro F.   +5 more
europepmc   +1 more source

A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation. [PDF]

Am J Case Rep, 2017
Arnautovic JZ, Mazhar A, Tereziu S, Gupta K.   +3 more
europepmc   +1 more source

Acute Cholecystitis in a Patient With Situs Inversus. [PDF]

Cureus
Althunayan SA, AlRubaysh NS, Alshaban JA, Ali SO.   +3 more
europepmc   +1 more source