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infantile kidney相关文献:
Differences in kidney prognosis between congenital and infantile nephrotic syndrome.
Inoki Y, Horinouchi T, Aoyama S, Kimura Y, Ichikawa Y, Tanaka Y, Ueda C, Kitakado H, Kondo A, Sakakibara N, Kamei K, Hamada R, Fujita N, Gotoh Y, Kaku Y, Nishiyama K, Okamoto T, Toya Y, Yamamura T, Ishimori S, Nagano C, Nozu K.
Pediatr Nephrol. 2025 Aug;40(8):2539-2549. doi: 10.1007/s00467-025-06735-z. Epub 2025 Mar 17.
PMID:40095038
Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia.
Gurevich E, Borovitz Y, Levi S, Perlman S, Landau D.
Pediatr Nephrol. 2023 Apr;38(4):1067-1073. doi: 10.1007/s00467-022-05740-w. Epub 2022 Sep 26.
PMID:36156733
Infantile nephrotic syndrome.
George CR, Hickman RO, Stricker GE.
Clin Nephrol. 1976 Jan;5(1):20-4.
PMID:765027
[Infantile polycystic kidney disease: a case report and literature review].
Luo F, Gu WZ, Chen Z, Shi LP, Ma XL, Lin HJ, Qiu YH.
Zhonghua Er Ke Za Zhi. 2013 May;51(5):377-81.
PMID:23941846
[Infantile polycystic kidney].
Barrera M, Quezada L.
Rev Chil Pediatr. 1986 Jan-Feb;57(1):35-8.
PMID:3532227
Chest configuration in children and adolescents with infantile nephropathic cystinosis compared with other chronic kidney disease entities and its clinical determinants.
Müller S, Kluck R, Jagodzinski C, Brügelmann M, Hohenfellner K, Büscher A, Kemper MJ, Fröde K, Oh J, Billing H, Thumfart J, Weber LT, Acham-Roschitz B, Arbeiter K, Tönshoff B, Hagenberg M, Pavičić L, Haffner D, Zivicnjak M.
Pediatr Nephrol. 2023 Dec;38(12):3989-3999. doi: 10.1007/s00467-023-06058-x. Epub 2023 Jul 7.
PMID:37415042
Beneficial effects of starting oral cysteamine treatment in the first 2 months of life on glomerular and tubular kidney function in infantile nephropathic cystinosis.
Hohenfellner K, Nießl C, Haffner D, Oh J, Okorn C, Palm K, Schlingmann KP, Wygoda S, Gahl WA.
Mol Genet Metab. 2022 Aug;136(4):282-288. doi: 10.1016/j.ymgme.2022.06.009. Epub 2022 Jul 1.
PMID:35843134
Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.
Nießl C, Boulesteix AL, Oh J, Palm K, Schlingmann P, Wygoda S, Haffner D, Wühl E, Tönshoff B, Buescher A, Billing H, Hoppe B, Zirngibl M, Kettwig M, Moeller K, Acham-Roschitz B, Arbeiter K, Bald M, Benz M, Galiano M, John-Kroegel U, Klaus G, Marx-Berger D, Moser K, Mueller D, Patzer L, Pohl M, Seitz B, Treikauskas U, von Vigier RO, Gahl WA, Hohenfellner K.
Mol Genet Metab. 2022 Aug;136(4):268-273. doi: 10.1016/j.ymgme.2022.06.010. Epub 2022 Jul 2.
PMID:35835062
Autosomal Recessive Polycystic Kidney Disease.
Subramanian S, Leslie SW, Ahmad T.
2024 Mar 3. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–.
PMID:30725822
More than tubular dysfunction: cystinosis and kidney outcomes.
Atmis B, K Bayazit A, Cevizli D, Kor D, Fidan HB, Bisgin A, Kilavuz S, Unal I, Erdogan KE, Melek E, Gonlusen G, Anarat A, Onenli Mungan N.
J Nephrol. 2022 Apr;35(3):831-840. doi: 10.1007/s40620-021-01078-y. Epub 2021 Jun 7.
PMID:34097292
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