Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

207 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Renal glucosuria.
Brodehl J, Oemar BS, Hoyer PF. Brodehl J, et al. Pediatr Nephrol. 1987 Jul;1(3):502-8. doi: 10.1007/BF00849261. Pediatr Nephrol. 1987. PMID: 3153324 Review.
The plasma concentration and renal handling of taurine in healthy children and in pediatric patients with disturbed sulfur metabolism.
Rödenbeck D, Byrd DJ, Brodehl J. Rödenbeck D, et al. Among authors: brodehl j. Adv Exp Med Biol. 1994;359:399-403. doi: 10.1007/978-1-4899-1471-2_41. Adv Exp Med Biol. 1994. PMID: 7887280 No abstract available.
Evidence suggesting hyperoxaluria as a cause of nephrocalcinosis in phosphate-treated hypophosphataemic rickets.
Reusz GS, Latta K, Hoyer PF, Byrd DJ, Ehrich JH, Brodehl J. Reusz GS, et al. Among authors: brodehl j. Lancet. 1990 May 26;335(8700):1240-3. doi: 10.1016/0140-6736(90)91304-s. Lancet. 1990. PMID: 1971321
Association of spondylo-epiphyseal dysplasia with nephrotic syndrome.
Ehrich JH, Offner G, Schirg E, Hoyer PF, Helmchen U, Brodehl J. Ehrich JH, et al. Among authors: brodehl j. Pediatr Nephrol. 1990 Mar;4(2):117-21. doi: 10.1007/BF00858821. Pediatr Nephrol. 1990. PMID: 2397176
Molecular analysis of the SGLT2 gene in patients with renal glucosuria.
Santer R, Kinner M, Lassen CL, Schneppenheim R, Eggert P, Bald M, Brodehl J, Daschner M, Ehrich JH, Kemper M, Li Volti S, Neuhaus T, Skovby F, Swift PG, Schaub J, Klaerke D. Santer R, et al. Among authors: brodehl j. J Am Soc Nephrol. 2003 Nov;14(11):2873-82. doi: 10.1097/01.asn.0000092790.89332.d2. J Am Soc Nephrol. 2003. PMID: 14569097 Free article.
Autosomal recessive and dominant forms of polycystic kidney disease are not allelic.
Wirth B, Zerres K, Fischbach M, Claus D, Neumann HP, Lennert T, Brodehl J, Neugebauer M, Müller-Wiefel DE, Geisert J, et al. Wirth B, et al. Among authors: brodehl j. Hum Genet. 1987 Nov;77(3):221-2. doi: 10.1007/BF00284473. Hum Genet. 1987. PMID: 3479385
Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria.
Langen H, von Kietzell D, Byrd D, Arslan-Kirchner M, Vester U, Stuhrmann M, Dörk T, Saar K, Reis A, Schmidtke J, Brodehl J. Langen H, et al. Among authors: brodehl j. Pediatr Nephrol. 2000 May;14(5):376-84. doi: 10.1007/s004670050778. Pediatr Nephrol. 2000. PMID: 10805464 Free PMC article.
Distal myopathy in nephropathic cystinosis.
Vester U, Schubert M, Offner G, Brodehl J. Vester U, et al. Among authors: brodehl j. Pediatr Nephrol. 2000 Jan;14(1):36-8. doi: 10.1007/s004670050009. Pediatr Nephrol. 2000. PMID: 10654328 Clinical Trial.
In what order should one introduce cyclophosphamide or chlorambucil, cyclosporine or levamisole in a child with steroid-dependent frequently relapsing nephrotic syndrome?
Brodehl J. Brodehl J. Pediatr Nephrol. 1993 Oct;7(5):514. doi: 10.1007/BF00852529. Pediatr Nephrol. 1993. PMID: 8251311 No abstract available.
Improved absorption of cyclosporin A from a new microemulsion formulation: implications for dosage and monitoring.
Bökenkamp A, Offner G, Hoyer PF, Vester U, Wonigeit K, Brodehl J. Bökenkamp A, et al. Among authors: brodehl j. Pediatr Nephrol. 1995 Apr;9(2):196-8. doi: 10.1007/BF00860745. Pediatr Nephrol. 1995. PMID: 7794718 Clinical Trial.
207 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback