Results 151 to 160 of about 8,550 (230)

Whole-exome sequencing in pediatric patients with glomerulonephritis. [PDF]

Front Genet
Peric M, Brankovic M, Stajic N, Putnik J, Paripovic A, Jankovic M, Nikolic D, Milanovic F, Novakovic I, Vukomanovic V.   +9 more
europepmc   +1 more source

HEREDITARY FAMILIAL NEPHRITIS

Nihon Naika Gakkai Zasshi, 1972
HASHIMOTO, Yasuo, MORI, Mayumi, KANAZAWA, Ichiro, ISHIKAWA, Tadashi, TANAKA, Toshiyuki, DOFUKU, Ryuichi, KINUGASA, Keiji, SUGANO, Haruo, TAKUMA, Takehide   +8 more
openaire   +2 more sources

Phenotype of autosomal dominant Alport syndrome with a likely pathogenic heterozygous variant in the COL4A3 gene (Gly366Arg) and incidental teratozoospermia: A case report. [PDF]

An Sist Sanit Navar
Martín Moreno V, Martín Fernández A, García Mateos A, Hurtado Gallar J, Angulo García C, Sánchez-Redondo Mayordomo R.   +5 more
europepmc   +1 more source

Hereditary transthyretin amyloidosis mimicking ALS: First genetically proven case report from Saudi Arabia. [PDF]

eNeurologicalSci
Elshony H, Almuhanna R, Albazli KO, Muddassir R.   +3 more
europepmc   +1 more source

Case report: Surgical and clinical results in bilateral lenticonus due to Alport syndrome. [PDF]

Rom J Ophthalmol
Çakmak-Cengiz E, Karaman-Atasever F, Can E.   +2 more
europepmc   +1 more source

miRNAs in Glomerular Diseases: From Pathogenic Insight to Therapeutic Potential: A Narrative Review. [PDF]

Cells
Apetrii M, Costache AD, Costache Enache II, Voroneanu L, Covic AS, Kanbay M, Scripcariu DV, Covic A.   +7 more
europepmc   +1 more source

A rare case of dual glomerular pathology: Alport syndrome and immune complex-mediated MPGN. [PDF]

BMC Nephrol
Ozcan SG, Koc E, Murt A, Dincer MT, Gurses I, Seyahi N, Trabulus S.   +6 more
europepmc   +1 more source

The immunomodulatory potential of bradykinin signaling in autoimmune conditions. [PDF]

Front Immunol
Szaryńska M, Olejniczak-Kęder A.
europepmc   +1 more source

Clinical features of hearing loss and genotype-phenotype correlations in Alport syndrome caused by COL4A4 or COL4A5 variants. [PDF]

Sci Rep
Matsuzaki S, Nara K, Mutai H, Katsunuma S, Sakamoto H, Hirose M, Wakisaka N, Adachi N, Asanuma S, Fujioka M, Matsunaga T.   +10 more
europepmc   +1 more source

Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis. [PDF]

Int J Lab Hematol
Melo MAW, Silveira CM, Ribeiro MM, Arcanjo GS.   +3 more
europepmc   +1 more source