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2. Galactose metabolism in a patient with hereditary galactokinase deficiency. Gitzelmann R; Wells HJ; Segal S Eur J Clin Invest; 1974 Apr; 4(2):79-84. PubMed ID: 4365005 [No Abstract] [Full Text] [Related]
3. [Isotope use in the study of hereditary metabolic diseases]. Linneweh F Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):191-4. PubMed ID: 4943517 [No Abstract] [Full Text] [Related]
7. [Hereditary deficiency of 1 -antitrypsin]. Dautrevaux M Lille Med; 1971 Oct; 16(8):1113-21. PubMed ID: 5120783 [No Abstract] [Full Text] [Related]
8. Nonhemolytic unconjugated hyperbilirubinemia with hepatic glucuronyl transferase deficiency: a genetic study in four generations. Sleisenger MH Trans Assoc Am Physicians; 1967; 80():259-66. PubMed ID: 6082246 [No Abstract] [Full Text] [Related]
10. Carbamylphosphate synthetase deficiency in an infant with severe cerebral damage. Hommes FA; De Groot CJ; Wilmink CW; Jonxis JH Arch Dis Child; 1969 Dec; 44(238):688-93. PubMed ID: 5356974 [No Abstract] [Full Text] [Related]
11. Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency. Violi F; Sanguigni V; Loffredo L; Carnevale R; Buchetti B; Finocchi A; Tesauro M; Rossi P; Pignatelli P Arterioscler Thromb Vasc Biol; 2006 Aug; 26(8):e131-2. PubMed ID: 16857955 [No Abstract] [Full Text] [Related]
12. The pattern of lung disease associated with alpha antitrypsin deficiency. Guenter CA; Welch MH; Russell TR; Hyde RM; Hammarsten JF Arch Intern Med; 1968 Sep; 122(3):254-7. PubMed ID: 5671106 [No Abstract] [Full Text] [Related]
14. [Various remarks on the pathological anatomy of hereditary metabolic disorders]. Huber J Midwives Chron; 1967 Sep; ():360-5. PubMed ID: 5182851 [No Abstract] [Full Text] [Related]
15. The field investigation for acatalasemic gene carriers. Wakisaka G; Yamamoto T; Yamamoto Y; Sakamoto K; Sawada M Naika Hokan; 1967 May; 14(5):151-7. PubMed ID: 5624288 [No Abstract] [Full Text] [Related]
16. [Genetic heterogeneity of hereditary enzymopathies]. Krasnopol'skaia KD; Bochkov NP Vestn Akad Med Nauk SSSR; 1982; (9):56-64. PubMed ID: 7148122 [No Abstract] [Full Text] [Related]
17. [Pendred's syndrome and goiter endemia]. Ferraris GM; Zoppetti G; Bidone G; Costa A Folia Endocrinol; 1966 Jun; 19(3):295-312. PubMed ID: 6012940 [No Abstract] [Full Text] [Related]
18. [Biochemical characteristics and diagnosis of lysosomal diseases related to hereditary glycosidase deficiency]. Vidershaĭn GIa Vestn Akad Med Nauk SSSR; 1982; (6):42-7. PubMed ID: 6810572 [No Abstract] [Full Text] [Related]
19. [Familial plasma cholesterol ester deficiency. A new inborn error of metabolism]. Gjone E; Norum KR Nord Med; 1968 Jul; 80(27):878-83. PubMed ID: 5685656 [No Abstract] [Full Text] [Related]
20. [On a new case of congenital methemoglobinemia caused by deficiency of diaphorease with grave cerebropathy]. Ronconi G; Ferracin G Fracastoro; 1968; 61(2):121-8. PubMed ID: 5704045 [No Abstract] [Full Text] [Related] [Next] [New Search]