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7. Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy. Whitehouse DB; Lovegrove JU; Hopkinson DA Clin Chim Acta; 1989 Jan; 179(1):109-15. PubMed ID: 2784082 [TBL] [Abstract][Full Text] [Related]
8. Pi Ecincinnati: a new alpha 1-antitrypsin allele in three Negro families. Hug G; Chuck G; Slemmer TM; Fagerhol MK Hum Genet; 1980; 54(3):361-4. PubMed ID: 6967446 [TBL] [Abstract][Full Text] [Related]
9. The microheterogeneities of thyroxine-binding globulin and alpha 1 protease inhibitor (alpha 1-antitrypsin) are interrelated. Beilby JP; Dick M; Kay P; Watson FE Clin Chim Acta; 1983 Sep; 133(1):51-63. PubMed ID: 6414740 [TBL] [Abstract][Full Text] [Related]
10. Glycogen storage disease in Israel. A clinical, biochemical and genetic study. Levin S; Moses SW; Chayoth R; Jagoda N; Steinitz K Isr J Med Sci; 1967; 3(3):397-410. PubMed ID: 5317551 [No Abstract] [Full Text] [Related]
11. Alpha-1-antitrypsin: evidence for a fifth PI M subtype and a new deficiency allele PI*Z augsburg. Weidinger S; Jahn W; Cujnik F; Schwarzfischer F Hum Genet; 1985; 71(1):27-9. PubMed ID: 3875547 [TBL] [Abstract][Full Text] [Related]
12. Liver disease and the PI ElembergM phenotype of alpha 1-antitrypsin. Berninger RW; DeLellis RA; Kaplan MM Am J Clin Pathol; 1985 Apr; 83(4):503-6. PubMed ID: 3885715 [TBL] [Abstract][Full Text] [Related]
14. Genetic polymorphism of serum alpha-1-protease inhibitor (alpha-1-antitrypsin): Pi i, a deficient allele of the Pi system. Arnaud P; Chapuis-Cellier C; Vittoz P; Fudenberg HH J Lab Clin Med; 1978 Aug; 92(2):177-84. PubMed ID: 308085 [TBL] [Abstract][Full Text] [Related]
15. Human alpha 1-antitrypsin genetic polymorphism: PI N subtypes. Sesboüé R; Vercaigne D; Charlionet R; Lefebvre F; Martin JP Hum Hered; 1984; 34(2):105-13. PubMed ID: 6611291 [TBL] [Abstract][Full Text] [Related]
16. Alpha-1-antitrypsin phenotypes in malignant lymphoma. Callea F; Massi G; De Wolf-Peeters C; Lievens C; Desmet VJ J Clin Pathol; 1982 Nov; 35(11):1213-5. PubMed ID: 6982905 [TBL] [Abstract][Full Text] [Related]
17. [Mutation in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China]. Qiu ZQ; Lu CX; Wang W; Qiu JJ; Wei M Zhonghua Er Ke Za Zhi; 2011 Mar; 49(3):203-8. PubMed ID: 21575371 [TBL] [Abstract][Full Text] [Related]
18. Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants. Skakic A; Djordjevic M; Sarajlija A; Klaassen K; Tosic N; Kecman B; Ugrin M; Spasovski V; Pavlovic S; Stojiljkovic M Clin Genet; 2018 Feb; 93(2):350-355. PubMed ID: 28685844 [TBL] [Abstract][Full Text] [Related]
19. Glycogen storage disease type Ib without neutropenia generated by a novel splice-site mutation in the glucose-6-phosphate translocase gene. Angaroni CJ; Labrune P; Petit F; Sastre D; Capra AE; Dodelson de Kremer R; Argaraña CE Mol Genet Metab; 2006 May; 88(1):96-9. PubMed ID: 16490377 [TBL] [Abstract][Full Text] [Related]
20. [Determination of alpha 1 antitrypsin phenotypes in plasma using isoelectric focusing on this agarose gel]. Renversez JC; Lebrun-Fourcy C; Rondot J; Revol C Pathol Biol (Paris); 1998 Jan; 46(1):15-20. PubMed ID: 9769931 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]