Personal information

Activities

Employment (2)

Hyogo Prefectural Kobe Children’s Hospital: Kobe, JP

2019-04-01 to present (General Pediatrics)
Employment
Source: Self-asserted source
Shogo Minamikawa

Kobe University: Kobe, JP

2014-04-01 to present
Employment
Source: Self-asserted source
Shogo Minamikawa

Education and qualifications (2)

Kobe University: Kobe, JP

2014-04-01 to 2018-03-31 | PhD (Pediatrics)
Qualification
Source: Self-asserted source
Shogo Minamikawa

Mie Daigaku: Tsu, Mie, JP

2003-04-01 to 2009-03-31
Education
Source: Self-asserted source
Shogo Minamikawa

Funding (3)

気管切開児における下気道細菌感染症の臨床的・血液学的特徴の解明

2020-04 to 2021-03 | Grant
Japan Society for the Promotion of Science (Tokyo, JP)
Source: Self-asserted source
Shogo Minamikawa

患者由来近位尿細管細胞を用いたLowe症候群の病態解明および新規治療法の開発

2017-04-01 to 2020-03-31 | Grant
Japan Society for the Promotion of Science (Tokyo, JP)
GRANT_NUMBER: 17K16087
Source: Self-asserted source
Shogo Minamikawa via DimensionsWizard

Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome

2016-04-01 to 2018-03-31 | Grant
Japan Society for the Promotion of Science (Tokyo, JP)
GRANT_NUMBER: 16K19642
Source: Self-asserted source
Shogo Minamikawa via DimensionsWizard

Works (44)

A Case of Cefotaxime-induced Drug Reaction with Eosinophilia and Systemic Symptoms

2024-09-16 | Preprint
Contributors: Chiaki Masuda; Shogo Minamikawa; Tomohiro Hasegawa; Sayaka Okazaki; Kana Hamada; Yasuo Nakagishi
Source: check_circle
Crossref

A Pediatric Case of Panniculitis Induced by Pseudomonas Aeruginosa With Clinical Features Similar to Ecthyma Gangrenosum

Pediatric Infectious Disease Journal
2024-07 | Journal article
Contributors: Urara Saito; Shogo Minamikawa; Shogo Otake; Yusuke Ishida; Mao Mizuta; Toshiaki Ishida; Shuhei Karakawa; Masashi Kasai; Yasuo Nakagishi
Source: check_circle
Crossref

Delayed pneumomediastinum following oropharyngeal injury: A report of two pediatric cases

Trauma
2023-07 | Journal article
Contributors: Yukari Aida; Shogo Minamikawa; Mao Mizuta; Shogo Otake; Yasuo Nakagishi
Source: check_circle
Crossref

Painless subcutaneous abscess caused by bacillus Calmette–Guérin osteomyelitis

Pediatrics International
2023-01 | Journal article
Contributors: Osamu Matsumura Momo; Shogo Otake; Shogo Minamikawa; Kiyofumi Ohkusu; Yasuo Nakagishi
Source: check_circle
Crossref

A Case of Influenza Virus-Induced Acute Cerebellitis Treated with Steroid Pulse Therapy

Journal of Pediatric Neurology
2022-06 | Journal article
Contributors: Yukiho Hirota; Shogo Minamikawa; Yusuke Ishida; Azusa Maruyama; Yasuo Nakagishi
Source: check_circle
Crossref

Conservative treatment for an anterior cutaneous nerve entrapment syndrome case

Pediatrics International
2022-01 | Journal article
Contributors: Shogo Minamikawa; Eri Ueshima; Akiko Yokoi; Yusuke Ishida; Yasuo Nakagishi
Source: check_circle
Crossref

Sciatic neuropathy caused by forced stretching exercise

Pediatrics International
2022-01 | Journal article
Contributors: Yoshitaka Asagai; Shogo Minamikawa; Eri Ueshima; Yukari Aida; Yasuo Nakagishi
Source: check_circle
Crossref

A pediatric case of tocilizumab‐resistant TAFRO syndrome treated successfully with rituximab

Pediatric Blood & Cancer
2020-12 | Journal article
Contributors: Shogo Minamikawa; Osamu Matsumura; Seiko Sato; Yasuo Nakagishi; Ryojiro Tanaka
Source: check_circle
Crossref

Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2.

Pediatric nephrology (Berlin, Germany)
2020-07-18 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Pathogenic evaluation of synonymous COL4A5 variants in X-linked Alport syndrome using a minigene assay.

Molecular genetics & genomic medicine
2020-06-16 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.

Kidney international
2020-06-14 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.

Nature communications
2020-06-02 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Gastrointestinal symptoms as an extended clinical feature of Pierson syndrome: a case report and review of the literature.

BMC medical genetics
2020-04-15 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Clinical and genetic variability of PAX2-related disorder in the Japanese population.

Journal of human genetics
2020-03-16 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Molecular mechanisms determining severity in patients with Pierson syndrome.

Journal of human genetics
2020-01-21 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay.

Scientific reports
2019-09-03 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.

Molecular genetics & genomic medicine
2019-07-30 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Clinical characteristics of HNF1B-related disorders in a Japanese population.

Clinical and experimental nephrology
2019-05-27 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome.

Journal of human genetics
2019-04-23 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.

Clinical and experimental nephrology
2018-12-24 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases.

Scientific reports
2018-11-23 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Clinical spectrum of male patients with OFD1 mutations.

Journal of human genetics
2018-11-06 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome.

Kidney international reports
2018-09-28 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry.

Case reports in nephrology and dialysis
2018-09-25 | Journal article
Source: Self-asserted source
Shogo Minamikawa

A review of clinical characteristics and genetic backgrounds in Alport syndrome.

Clinical and experimental nephrology
2018-08-20 | Journal article
Source: Self-asserted source
Shogo Minamikawa

TGFBI-associated corneal dystrophy and nephropathy: a novel syndrome?

CEN case reports
2018-08-07 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.

Journal of the American Society of Nephrology : JASN
2018-06-29 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.

Journal of human genetics
2018-05-30 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes.

Journal of human genetics
2018-03-19 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease.

Journal of human genetics
2018-02-19 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.

Clinical and experimental nephrology
2018-01-25 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits.

Nephron
2017-11-03 | Journal article
Source: Self-asserted source
Shogo Minamikawa

A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome.

European journal of medical genetics
2017-08-09 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome.

Kidney international reports
2017-05-04 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical center.

Environmental health and preventive medicine
2017-03-31 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.

Journal of human genetics
2017-03-09 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Diagnostic strategy for inherited hypomagnesemia.

Clinical and experimental nephrology
2017-03-01 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Clinical characteristics and long-term outcome of diarrhea-associated hemolytic uremic syndrome: a single center experience.

Clinical and experimental nephrology
2017-01-10 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Female X-linked Alport syndrome with somatic mosaicism.

Clinical and experimental nephrology
2016-10-31 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Cryptic exon activation in SLC12A3 in Gitelman syndrome.

Journal of human genetics
2016-10-27 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.

Clinical journal of the American Society of Nephrology : CJASN
2016-06-08 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.

Clinical and experimental nephrology
2016-03-11 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.

Clinical and experimental nephrology
2015-09-01 | Journal article
Source: Self-asserted source
Shogo Minamikawa

Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.

Genetics in medicine : official journal of the American College of Medical Genetics
2015-04-16 | Journal article
Source: Self-asserted source
Shogo Minamikawa
grade
Preferred source (of 2)‎

Peer review (2 reviews for 2 publications/grants)

Review activity for BMC nephrology (1)
Review activity for CEN case reports. (1)