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Items: 1 to 20 of 96

1.

Hereditary variants of serum alpha-1-antitrypsin.

Axelsson U, Laurell CB.

Am J Hum Genet. 1965 Nov;17(6):466-72. No abstract available.

2.

Alpha-1-antitrypsin deficiency and chronic pulmonary disease.

Erkstam G, Kiviloog J, Ostling E.

Scand J Respir Dis. 1968;49(4):311-21. No abstract available.

PMID:
4185284
3.

[A CASE OF FAMILIAL ALPHA-1-ANTITRYPSIN DEFICIENCY].

LOPEZ V, OETLIKER O, COLOMBO JP, BUETLER R.

Helv Paediatr Acta. 1964 Oct;19:296-303. German. No abstract available.

PMID:
14229909
4.

[ALPORT'S SYNDROME OR HEREDITARY CHRONIC NEPHRITIS].

PETERS R.

Maandschr Kindergeneeskd. 1964 Jan;32:18-28. Dutch. No abstract available.

PMID:
14162584
5.

SERUM PROTEIN ELECTROPHORETIC FRACTIONS AMONG NEGRO AND WHITE SUBJECT IN EVANS COUNTY, GEORGIA.

LICHTMAN MA, HAMES CG, MCDONOUGH JR.

Am J Clin Nutr. 1965 Jun;16:492-508. No abstract available.

PMID:
14297282
6.

Studies in alpha 1-antitrypsin deficiency.

Eriksson S.

Acta Med Scand Suppl. 1965;432:1-85. No abstract available.

PMID:
4160491
7.

SERUM LIPOPROTEINS & CHOLESTEROL METABOLISM IN XERODERMA PIGMENTOSUM.

EL-HEFNAWI H, ABDEL-GAWAD Z, HASSAN F, EL-MARSAFY MK.

J Egypt Med Assoc. 1963;46:1041-50. No abstract available.

PMID:
14162089
8.

Hereditary alpha-1-antitrypsin deficiency.

Talamo RC, Allen JD, Kahan MG, Auste KF.

N Engl J Med. 1968 Feb 15;278(7):345-51. No abstract available.

PMID:
4169707
9.

Serum proteins: diagnostic significance of electrophoretic patterns.

Larson PH.

Hum Pathol. 1974 Nov;5(6):629-40. Review. No abstract available.

PMID:
4138596
10.

HYPOGAMMAGLOBULINEMIA; IODINATED GAMMA GLOBULIN STUDIES.

PRASAD AS, ABOUD MA, SALAWI A, SCHULERT AR.

Ann Intern Med. 1964 Aug;61:319-25. No abstract available.

PMID:
14204868
11.

Heterozygous and homozygous alpha1-antitrypsin deficiency in patients with pulmonary emphysema.

Lieberman J.

N Engl J Med. 1969 Aug 7;281(6):279-84. No abstract available.

PMID:
4183173
12.

Familial emphysema associated with antitrypsin deficiency.

Kowalyshyn T, Sataline LR.

Dis Chest. 1969 Apr;55(4):285-9. No abstract available.

PMID:
4180351
13.

Steroid-protein interactions. XI. Electrophoretic characterization of corticosteroid-binding proteins in serum of rat, man and other species.

Westphal U, Devenuto F.

Biochim Biophys Acta. 1966 Jan 25;115(1):187-96. No abstract available.

PMID:
4160735
14.

A FAMILY STUDY OF IDIOPATHIC PULMONARY FIBROSIS: A POSSIBLE DYSPROTEINEMIC AND GENETICALLY DETERMINED DISEASE.

JACOX RF, FRYMOYER J, BONANNI P.

Trans Assoc Am Physicians. 1964;77:232-8. No abstract available.

PMID:
14275423
15.

[A STUDY ON THE MECHANISM OF CYSTITIS COLIGENES ESPECIALLY ON DIFFERENCE OF GLOBULIN].

IWATA S.

Nihon Hinyokika Gakkai Zasshi. 1964 Mar;55:275-7. Japanese. No abstract available.

PMID:
14173345
16.

[Alpha-1-antitrypsin deficiency associated with chronic bronchopneumopathy and essential emphysema].

Brun J, Biot N, Kofman J, Perrin-Fayolle M.

Poumon Coeur. 1967;23(9):1119-30. French. No abstract available.

PMID:
4176461
17.

[Catabolism of I-131 serum proteins by polymorphonucleated leukocytes in vitro. 3. Study with alpha-2 and beta-globulins].

Viti A, Pacini A, Bocci V.

Boll Soc Ital Biol Sper. 1967 Nov 30;43(22):1559-62. Italian. No abstract available.

PMID:
4175645
18.

[Alpha 1-globulin analysis as a screening test for congenital alpha 1-antitrypsin deficiency].

Rujner J.

Pol Tyg Lek. 1988 Jun 20;43(25):811-3. Polish. No abstract available.

PMID:
2468152
19.

[Electrophoretic study in rheumatoid disease. 3. Alpha and beta globulins].

Cossermelli W.

Rev Hosp Clin Fac Med Sao Paulo. 1968 Jul;23(4):175-82. Portuguese. No abstract available.

PMID:
4175979
20.

Investigations on ceruloplasmin in chronic schizophrenia.

PuzyƄski S.

Pol Med J. 1966;5(6):1484-91. No abstract available.

PMID:
4166118

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