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CEN Case Reports
|
June 29, 2026
Pediatric case of anti-neutrophil cytoplasmic antibody-associated glomerulonephritis with immunoglobulin a deposition diagnosed early through school urinary screening
Takuto Kawamura, Yuko Kajiho, Keiichi Takizawa, et al.
Molecular Biology of the Cell
|
April 8, 2011
Tyrosine phosphorylation-dependent activation of TRPC6 regulated by PLC-γ1 and nephrin: effect of mutations associated with focal segmental glomerulosclerosis
Shoichiro Kanda, Yutaka Harita, Yoshio Shibagaki, et al.
CEN Case Reports
|
September 2, 2022
A case of right hypodysplastic kidney and ectopic ureter associated with bicornuate uterus in a prepubertal girl
Misako Nakamura, Shoichiro Kanda, Yuko Kajiho, et al.
Cureus
|
November 7, 2025
A Case of Type 1 Congenital Pulmonary Airway Malformation (CPAM) in an Eight-Year-Old Girl Without a History of Recurrent Pneumonia or Respiratory Failure, Presenting With a Pulmonary Abscess
Ryutaro Ohira, Natsuho Adachi, Shoichiro Kanda, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
January 28, 2015
Gonadal tumor in Frasier syndrome: a review and classification
Jiro Ezaki, Kazunori Hashimoto, Tatsuo Asano, et al.
CEN Case Reports
|
January 24, 2020
Rituximab-induced serum sickness in a 6-year-old boy with steroid-dependent nephrotic syndrome
Misako Nakamura, Shoichiro Kanda, Yuya Yoshioka, et al.
CEN Case Reports
|
September 1, 2025
Successful kidney transplantation using eltrombopag in a patient with MYH9-related disease
Aya Kato, Yoko Shirai, Shoichiro Kanda, et al.
Journal of Human Genetics
|
May 20, 2020
Incomplete cryptic splicing by an intronic mutation of OCRL in patients with partial phenotypes of Lowe syndrome
Eiji Nakano, Amine Yoshida, Yudai Miyama, et al.
BMC Nephrology
|
December 21, 2021
A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report
Yoko Shirai, Kenichiro Miura, Naoto Kaneko, et al.
Nephrology (Carlton, Vic.)
|
December 8, 2023
Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome
Juri Kanda, Shoichiro Kanda, Yoshiki Hayashi, et al.
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Search research articles
Search
Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
CEN Case Reports
|
June 29, 2026
Pediatric case of anti-neutrophil cytoplasmic antibody-associated glomerulonephritis with immunoglobulin a deposition diagnosed early through school urinary screening
Takuto Kawamura, Yuko Kajiho, Keiichi Takizawa, et al.
Molecular Biology of the Cell
|
April 8, 2011
Tyrosine phosphorylation-dependent activation of TRPC6 regulated by PLC-γ1 and nephrin: effect of mutations associated with focal segmental glomerulosclerosis
Shoichiro Kanda, Yutaka Harita, Yoshio Shibagaki, et al.
CEN Case Reports
|
September 2, 2022
A case of right hypodysplastic kidney and ectopic ureter associated with bicornuate uterus in a prepubertal girl
Misako Nakamura, Shoichiro Kanda, Yuko Kajiho, et al.
Cureus
|
November 7, 2025
A Case of Type 1 Congenital Pulmonary Airway Malformation (CPAM) in an Eight-Year-Old Girl Without a History of Recurrent Pneumonia or Respiratory Failure, Presenting With a Pulmonary Abscess
Ryutaro Ohira, Natsuho Adachi, Shoichiro Kanda, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
January 28, 2015
Gonadal tumor in Frasier syndrome: a review and classification
Jiro Ezaki, Kazunori Hashimoto, Tatsuo Asano, et al.
CEN Case Reports
|
January 24, 2020
Rituximab-induced serum sickness in a 6-year-old boy with steroid-dependent nephrotic syndrome
Misako Nakamura, Shoichiro Kanda, Yuya Yoshioka, et al.
CEN Case Reports
|
September 1, 2025
Successful kidney transplantation using eltrombopag in a patient with MYH9-related disease
Aya Kato, Yoko Shirai, Shoichiro Kanda, et al.
Journal of Human Genetics
|
May 20, 2020
Incomplete cryptic splicing by an intronic mutation of OCRL in patients with partial phenotypes of Lowe syndrome
Eiji Nakano, Amine Yoshida, Yudai Miyama, et al.
BMC Nephrology
|
December 21, 2021
A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report
Yoko Shirai, Kenichiro Miura, Naoto Kaneko, et al.
Nephrology (Carlton, Vic.)
|
December 8, 2023
Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome
Juri Kanda, Shoichiro Kanda, Yoshiki Hayashi, et al.
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of 5