トップ >  学会・研究会 >  教室業績集 >  2024年 >  症例報告

症例報告

(和文)

 

(英文)

1. Maejima A, Okuno K, Miyaishi M, Kawaba D, Kakee S, Yamaga K, Namba N:

  Deep juvenile xanthogranuloma invading the left tensor fasciae latae muscle: a case report

  and a literature review 

  J Clin Exp Hematop. 2024. doi:10.3960/jslrt.24056

 

2. Senoo S, Fujimoto M, Yamaguchi Y, Osaki M, Hanaki K, Namba N:

  Switching to burosumab from conventional therapy in siblings with relatively well-controlled

  X-linked hypophosphatemia.

  Clin Pediatr Endocrinol. 33: 27-34, 2024

 

3. Muroga C, Yokoyama H, Kinoshita R, Fujimori D, Yamada Y, Okanishi T, Morisada N, Nozu K,

  Namba N:

  A child with TSC2/PKD1 contiguous gene deletion syndrome successfully treated with tolvaptan

  for rapidly enlarging renal cysts.

  CEN Case Rep. 13: 351-355, 2024

 

4. Yamada Y, Yokoyama H, Kinoshita R, Kitamoto K, Kawaba Y, Okada S, Horie T, Nagano C,

  Nozu K, Namba N

  Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused

  by paired box protein 2 gene variant.

  CEN Case Rep. 13: 204-208, 2024