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Gerald S Spear

Title(s)Professor Emeritus, Pathology
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(714) 456-6141
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Congenital Gaucher disease with nonimmune hydrops/erythroblastosis, infantile arterial calcification, and neonatal hepatitis/fibrosis. Clinicopathologic report with enzymatic and genetic analysis. Fetal Pediatr Pathol. 2007 May-Jun; 26(3):153-68. Spear GS, Beutler E, Hungs M. PMID: 17886025.
      View in: PubMed   Mentions:
    2. Parietal bone agenesis with gracile bones and splenic hypoplasia/aplasia: clinico-pathologic report and differential diagnosis with review of cranio-gracile bone syndromes, "osteocraniostenosis" and Kleeblattschädel. . 2006 Nov 01; 140(21):2341-8. Spear GS. PMID: 17036309.
      View in: PubMed   Mentions:
    3. Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology. . 2006 Jul 15; 140(14):1553-63. Elliott AM, Wilcox WR, Spear GS, Field FM, Steffensen TS, Friedman BD, Rimoin DL, Lachman RS. PMID: 16770805.
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    4. Postmortem DNA diagnosis of factor V Leiden in a neonate with systemic thrombosis and probable antithrombin deficiency. Obstet Gynecol. 1998 Oct; 92(4 Pt 2):702-5. Newman RS, Spear GS, Kirschbaum N. PMID: 9764672.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    5. Eosinophilic explant carditis with eosinophilia: ?Hypersensitivity to dobutamine infusion. J Heart Lung Transplant. 1995 Jul-Aug; 14(4):755-60. Spear GS. PMID: 7578186.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    6. Bile nephrosis in a neonate: sonographic findings of rapid kidney enlargement and increased echogenicity. AJR Am J Roentgenol. 1992 Sep; 159(3):628-30. Bruno MA, Spear GS, Dietrich RB, Pugh PA. PMID: 1503040.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Comment on "The clinical significance of the glomerular location of segmental lesions in focal glomerulosclerosis". Clin Nephrol. 1991 Aug; 36(2):105. Spear GS. PMID: 1934656.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. Diffuse mesangial sclerosis in a fetus. Clin Nephrol. 1991 Jul; 36(1):46-8. Spear GS, Steinhaus KA, Quddusi A. PMID: 1889151.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    9. Morphologic alterations and biochemical studies of the glomerular basement membrane in Alport syndrome. Contrib Nephrol. 1990; 80:41-6. Spear GS. PMID: 2282821.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Renal allografts in cystinosis and mesangial demography. Clin Nephrol. 1989 Dec; 32(6):256-61. Spear GS, Gubler MC, Habib R, Broyer M. PMID: 2612069.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    11. Dark cells of cystinosis: occurrence in renal allografts. Hum Pathol. 1989 May; 20(5):472-6. Spear GS, Gubler MC, Habib R, Broyer M. PMID: 2651282.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    12. 47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation. Am J Med Genet. 1988 Mar; 29(3):511-5. Spear GS, Porto M. PMID: 3376994.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    13. Achondrogenesis type I: delineation of further heterogeneity and identification of two distinct subgroups. J Pediatr. 1988 Jan; 112(1):23-31. Borochowitz Z, Lachman R, Adomian GE, Spear G, Jones K, Rimoin DL. PMID: 3275766.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    14. DMSO potentiates aminonucleoside of puromycin nephrosis in rats. J Pathol. 1987 Oct; 153(2):183-7. Spear GS, Nguyen D, Conklin S, Wikle JS, Fan J, Lan YH, Allen J, Reineck S. PMID: 3694323.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    15. Bilateral pulmonary agenesis and microphthalmia. Am J Med Genet Suppl. 1987; 3:379-82. Spear GS, Yetur P, Beyerlein RA. PMID: 3130872.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    16. Fetal gonadoblastoid testicular dysplasia. Hum Pathol. 1986 May; 17(5):531-3. Spear GS, Martin CG. PMID: 3699814.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    17. Hereditary nephritis (Alport's syndrome)-1983. Clin Nephrol. 1984 Jan; 21(1):3-6. Spear GS. PMID: 6705272.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    18. Prenatal diagnosis of cystinosis. N Engl J Med. 1974 Apr 18; 290(16):878-82. Schneider JA, Verroust FM, Kroll WA, Garvin AJ, Horger EO, Wong VG, Spear GS, Jacobson C, Pellett OL, Becker FL. PMID: 4816962.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    19. The pathology of the kidney in the Alport syndrome. Birth Defects Orig Artic Ser. 1974; 10(4):109-13. Spear GS. PMID: 4470885.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    20. Pathology of the kidney in cystinosis. Pathol Annu. 1974; 9(0):81-92. Spear GS. PMID: 4608768.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    21. The pathology of the kidney in cystinosis. Birth Defects Orig Artic Ser. 1974; 10(4):87-8. Spear GS. PMID: 4620308.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    22. Pathology of the kidney in Alport's syndrome. Pathol Annu. 1974; 9(0):93-138. Spear GS. PMID: 4422868.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    23. Editorial: Alport's syndrome: a consideration of pathogenesis. Clin Nephrol. 1973 Nov-Dec; 1(6):336-7. Spear GS. PMID: 4786573.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    24. Idiopathic hematuria of childhood. Pathologic findings in the kidney in six patients. Hum Pathol. 1973 Sep; 4(3):349-80. Spear GS, Roskes SD, Slusser RJ, Alsruhe JP. PMID: 4585701.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    25. The proximal tubule and the podocyte in cystinosis. Nephron. 1973; 10(1):57-60. Spear G. PMID: 4695165.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    26. Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus. Am J Pathol. 1972 Nov; 69(2):213-24. Spear GS, Slusser RJ. PMID: 4343992.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    27. Polykaryocytosis of the visceral glomerular epithelium in cystinosis with description of an unusual clinical variant. Johns Hopkins Med J. 1971 Aug; 129(2):83-99. Spear GS, Slusser RJ, Schulman JD, Alexander F. PMID: 5567604.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    28. Cystinosis. An ultrastructural and electron-probe study of the kidney with unusual findings. Arch Pathol. 1971 Mar; 91(3):206-21. Spear GS, Slusser RJ, Tousimis AJ, Taylor CG, Schulman JD. PMID: 4322430.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    29. Hereditary nephritis with nerve deafness. Immunofluorescent studies on the kidney, with a consideration of discordant immunoglobulin-complement immunofluorescent reactions. Am J Med. 1970 Jul; 49(1):52-63. Spear GS, Whitworth JM, Konigsmark BW. PMID: 4988191.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
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