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

78 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load.
Rampini S, Völlmin JA, Bosshard HR, Müller M, Curtius HC. Rampini S, et al. Pediatr Res. 1974 Jul;8(7):704-9. doi: 10.1203/00006450-197407000-00003. Pediatr Res. 1974. PMID: 4837567 No abstract available.
Determination of urinary aromatic acids by gas chromatography. Results from healthy infants and from patients with phenylketonuria.
Völlmin JA, Bosshard HR, Müller M, Rampini S, Curtius HC. Völlmin JA, et al. Among authors: rampini s. Z Klin Chem Klin Biochem. 1971 Sep;9(5):402-4. Z Klin Chem Klin Biochem. 1971. PMID: 5173517 No abstract available.
[Phenylketonuria and hyperphenylalaninemia].
Rampini S, Gitzelmann R, Curtius HC. Rampini S, et al. Helv Paediatr Acta. 1971;25:Suppl 25:17-8. Helv Paediatr Acta. 1971. PMID: 5129695 German. No abstract available.
Detection of heterozygotes for phenylketonuria by column chromatography and discriminatory analysis.
Rampini S, Anders PW, Curtius HC, Marthaler T. Rampini S, et al. Pediatr Res. 1969 Jul;3(4):287-97. doi: 10.1203/00006450-196907000-00004. Pediatr Res. 1969. PMID: 5807058 No abstract available.
[Congenital disorders of phenylalanine metabolism].
Rampini S. Rampini S. Schweiz Med Wochenschr. 1973 Apr 14;103(15):537-46. Schweiz Med Wochenschr. 1973. PMID: 4572324 Review. German. No abstract available.
[Heterozygote identification in phenylketonuria].
Rampini S, Anders PW, Curtius HC, Marthaler T. Rampini S, et al. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1968;43(3-4):suppl 102-3. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1968. PMID: 5761621 German. No abstract available.
Congenital pseudohypoaldosteronism: case report and review. Effect of indomethacin during sodium chloride depletion.
Rampini S, Furrer J, Keller HP, Bucher H, Zachmann M. Rampini S, et al. Helv Paediatr Acta. 1978 Jun;33(2):153-67. Helv Paediatr Acta. 1978. PMID: 659259
[Combination of metachromatic leucodystrophy and mucopolysaccharidosis: a disease entity (mucosulfatidosis)].
Rampini S, Isler W, Baerlocher K, Bischoff A, Ulrich J, Plüss HJ. Rampini S, et al. Helv Paediatr Acta. 1970 Nov;25(5):436-61. Helv Paediatr Acta. 1970. PMID: 4250178 German. No abstract available.
Mild form of the Hunter syndrome, indentity of the biochemical defect with the severe type.
Wiesmann UN, Rampini S. Wiesmann UN, et al. Among authors: rampini s. Helv Paediatr Acta. 1974 Apr;29(1):73-8. Helv Paediatr Acta. 1974. PMID: 4275601 No abstract available.
[Farber's disease (disseminated lipogranulomatosis). Clinical picture and summary of the chemical findings].
Rampini S, Clausen J. Rampini S, et al. Helv Paediatr Acta. 1967 Dec;22(6):500-15. Helv Paediatr Acta. 1967. PMID: 4232884 German. No abstract available.
78 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page