Ming Juan Ye
Overview
Explore the profile of Ming Juan Ye including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
16
Citations
286
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Hanafusa H, Yamaguchi H, Morisada N, Ye M, Oikawa S, Tokumoto S, et al.
Brain Behav
. 2025 Feb;
15(2):e70279.
PMID: 39915231
Purpose: Status epilepticus associated with fever (SEF) is often encountered in pediatric emergency departments, and some patients develop neurological emergencies, such as acute encephalopathy (AE). Although numerous genetic variants of...
2.
Hanafusa H, Yamaguchi H, Morisada N, Ye M, Matsumoto R, Nagase H, et al.
Hum Genome Var
. 2024 Mar;
11(1):17.
PMID: 38548773
Autosomal dominant polycystic kidney disease (ADPKD) is commonly caused by PKD1, and mosaic PKD1 variants result in milder phenotypes. We present the case of a 32 year-old male with chronic...
3.
Hanafusa H, Yamaguchi H, Kondo H, Nagasaka M, Ye M, Oikawa S, et al.
Brain Dev
. 2023 Feb;
45(6):317-323.
PMID: 36774261
Objective: Hemorrhagic shock and encephalopathy syndrome (HSES) is a serious condition that requires intensive care and is associated with a high mortality rate. However, its pathogenesis remains unclear. In the...
4.
Sakakibara N, Nozu K, Yamamura T, Horinouchi T, Nagano C, Ye M, et al.
J Hum Genet
. 2022 Feb;
67(7):427-440.
PMID: 35140360
Nephronophthisis is an autosomal-recessive kidney disease that is caused by abnormalities in primary cilia. Nephronophthisis-related ciliopathies (NPHP-RCs) are a common cause of end-stage kidney disease (ESKD) in children and adolescents....
5.
Tanaka Y, Morisada N, Suzuki T, Ohashi Y, Ye M, Nozu K, et al.
CEN Case Rep
. 2020 Oct;
10(2):184-188.
PMID: 33048330
We present a female patient with a dual genetic diagnosis of autosomal dominant tubulointerstitial kidney disease and KBG syndrome. The proband was an 18-year-old woman presenting with intellectual disability, renal...
6.
Yamamura T, Horinouchi T, Nagano C, Omori T, Sakakibara N, Aoto Y, et al.
Kidney Int
. 2020 Jul;
98(6):1605-1614.
PMID: 32712167
Early kidney failure in the hereditary type IV collagen disease, Alport syndrome, can be delayed by renin-angiotensin inhibitors. However, whether all patients and all different genotypes respond equally well to...
7.
Yamamura T, Horinouchi T, Adachi T, Terakawa M, Takaoka Y, Omachi K, et al.
Nat Commun
. 2020 Jun;
11(1):2777.
PMID: 32488001
Currently, there are no treatments for Alport syndrome, which is the second most commonly inherited kidney disease. Here we report the development of an exon-skipping therapy using an antisense-oligonucleotide (ASO)...
8.
Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations
Morisada N, Hamada R, Miura K, Ye M, Nozu K, Hattori M, et al.
CEN Case Rep
. 2020 Apr;
9(3):260-265.
PMID: 32253632
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive ciliopathy characterized by retinitis pigmentosa (RP), truncal obesity, cognitive impairment, hypogonadism in men, polydactyly, and renal abnormalities with severe renal dysfunction. Twenty-two...
9.
Hanafusa H, Morisada N, Nomura T, Kobayashi D, Akasaka Y, Ye M, et al.
Hum Genome Var
. 2019 Jul;
6:31.
PMID: 31263565
CLOVES syndrome is characterized by congenital lipomatous overgrowth, vascular malformation, epidermal nevi, and scoliosis/spinal malformation. It is caused by somatic mosaicism of gain-of-function variants of . Here, we describe a...
10.
Sakakibara N, Morisada N, Nozu K, Nagatani K, Ohta T, Shimizu J, et al.
J Hum Genet
. 2018 Nov;
64(1):3-9.
PMID: 30401917
Oral-facial-digital syndrome type 1 (OFD1) is a ciliopathy characterized by oral, facial, and digital malformations that are often accompanied by polycystic lesion of the kidney and central nervous involvement. OFD1...