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121 related items for PubMed ID: 4356449
1. Eosinophilic Pelger-Huët anomaly with myeloproliferative disorder. Kay NE, Nelson DA, Gottlieb AJ. Am J Clin Pathol; 1973 Nov; 60(5):663-8. PubMed ID: 4356449 [No Abstract] [Full Text] [Related]
2. Pseudo-Pelger-Huët anomaly in chronic lymphocytic leukemia. Kornberg A, Goldfarb A, Shalev O. Acta Haematol; 1981 Nov; 66(2):127-8. PubMed ID: 6794312 [Abstract] [Full Text] [Related]
3. Acquired Pelger-Huet anomaly associated with Mycoplasma pneumoniae pneumonia. van Hook L, Spivack C, Duncanson FP. Am J Clin Pathol; 1985 Aug; 84(2):248-51. PubMed ID: 4025231 [Abstract] [Full Text] [Related]
7. Transfer of Pelger-Huet anomaly by bone marrow transplantation. Barton AM, MacLeod BC, Thomas ED. Am J Hematol; 1982 Sep; 13(2):163-6. PubMed ID: 6753573 [No Abstract] [Full Text] [Related]
8. [Myelodysplastic syndrome in a patient with familial Pelger-Huet anomaly]. Hiraga H, Yabe H, Nagai K, Nakayama S. Rinsho Ketsueki; 1991 Nov; 32(11):1453-7. PubMed ID: 1758052 [Abstract] [Full Text] [Related]
9. [Morphological abnormalities of polymorphonuclear neutrophils during myeloproliferative disorders]. Muratore R, Follana R, Khayati A, Olmer J. Nouv Rev Fr Hematol; 1973 Nov; 13(3):376-80. PubMed ID: 4270593 [No Abstract] [Full Text] [Related]
10. Pelger-Huet anomaly of granulocytes in a patient with tuberculosis. Savage PJ, Dellinger RP, Barnes JV, Carruth CW. Chest; 1984 Jan; 85(1):131-2. PubMed ID: 6690241 [Abstract] [Full Text] [Related]
11. [Familial Pelger-Huet anomaly simulating pathological "left-shift" in the blood picture]. Augustyniak W, Hilt J, Romanowska-Górecka B. Wiad Lek; 1979 Nov 15; 32(22):1643-5. PubMed ID: 538918 [No Abstract] [Full Text] [Related]
12. Eosinophilic acquired Pelger-Huët anomaly in acute myeloblastic leukemia. A cytochemical study. Chilosi M, Fossaluzza V, Tosato F. Acta Haematol; 1979 Nov 15; 61(4):198-202. PubMed ID: 108899 [Abstract] [Full Text] [Related]
13. Acute lymphoblastic leukaemia in a child with familial Pelger-Huet anomaly. Oneson R, Sabio H, Innes DJ. Br J Haematol; 1987 Jun 15; 66(2):193-7. PubMed ID: 3475111 [Abstract] [Full Text] [Related]
15. Familial Pelger-Huet anomaly accompanied by tuberculosis and complicated by acute polyarthritis. Suzuki N, Yasutake T, Ushiyama O, Hiida M, Ohta A, Yamaguchi M. Scand J Rheumatol; 1995 Jul 15; 24(5):319-20. PubMed ID: 8533050 [Abstract] [Full Text] [Related]
16. Pelger-Huët anomaly mimicking 'shift to the left'. Shmuely H, Pitlik SD, Inbal A, Rosenfeld JB. Neth J Med; 1993 Jun 15; 42(5-6):168-70. PubMed ID: 8377874 [Abstract] [Full Text] [Related]
17. [Malabsorption syndrome in an infant with Pelger-Huet anomaly]. Kaczmarski M, Szałkowska E, Sobolewska A. Pol Tyg Lek; 1982 Jul 05; 37(21):613-4. PubMed ID: 7145757 [No Abstract] [Full Text] [Related]
18. Epidermolysis bullosa dystrophica, hypoplastic type, associated with Pelger-Huet anomaly. Cat I, Marinoni LP, Giraldi DJ, Furtado de VP, Rasquini R, Freire-Maia N, Braga H. J Med Genet; 1967 Dec 05; 4(4):302-3. PubMed ID: 6082912 [No Abstract] [Full Text] [Related]
19. Acquired Pelger-Huët anomaly limited to eosinophils. Fossaluzza V, Tosato F. Acta Haematol; 1980 Dec 05; 63(5):295. PubMed ID: 6774561 [No Abstract] [Full Text] [Related]
20. Tuberculosis and Pelger-Huët anomaly. Case report. Cicchitto G, Parravicini M, De Lorenzo S, Di Pisa G, Malacrida A. Panminerva Med; 1999 Dec 05; 41(4):367-9. PubMed ID: 10705722 [Abstract] [Full Text] [Related] Page: [Next] [New Search]