Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 288

1.

Pelger-Huët anomaly: a critical review of the literature.

Speeckaert MM, Verhelst C, Koch A, Speeckaert R, Lacquet F.

Acta Haematol. 2009;121(4):202-6. doi: 10.1159/000220333. Epub 2009 May 26. Review.

PMID:
19468205
2.

Historical perspective and clinical implications of the Pelger-Hüet cell.

Cunningham JM, Patnaik MM, Hammerschmidt DE, Vercellotti GM.

Am J Hematol. 2009 Feb;84(2):116-9. doi: 10.1002/ajh.21320.

3.

[Nuclear abnormalities in Pelger-Huet anomaly; progress in blood cell morphology].

Tomonaga M.

Rinsho Byori. 2005 Jan;53(1):54-60. Review. Japanese.

PMID:
15724491
4.

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).

Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, Karl H, Kaps R, Müller D, Vayá A, Aznar J, Ware RE, Sotelo Cruz N, Lindner TH, Herrmann H, Reis A, Sperling K.

Nat Genet. 2002 Aug;31(4):410-4. Epub 2002 Jul 15.

PMID:
12118250
5.

Understanding and recognizing the Pelger-Huët anomaly.

Colella R, Hollensead SC.

Am J Clin Pathol. 2012 Mar;137(3):358-66. doi: 10.1309/AJCP3G8MDUXYSCID. Review.

PMID:
22338047
6.

Lamin B-receptor mutations in Pelger-Huët anomaly.

Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC.

Br J Haematol. 2003 Nov;123(3):542-4.

PMID:
14617022
7.

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.

Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K.

Hum Mol Genet. 2003 Jan 1;12(1):61-9.

PMID:
12490533
8.

Pelger-Huët anomaly in a child with 1q42.3-44 deletion.

Kalfa TA, Zimmerman SA, Goodman BK, McDonald MT, Ware RE.

Pediatr Blood Cancer. 2006 May 1;46(5):645-8.

PMID:
16007606
9.

[The Pelger-Huët anomaly. A clinical and ultrastructural study of a family from northeastern Mexico].

Sotelo-Cruz N, González-Olivas A, Covarrubias-Espinoza G, Lira Garcés JL, Valencia-Mayoral P.

Bol Med Hosp Infant Mex. 1991 Apr;48(4):261-6. Spanish.

PMID:
1867747
10.

[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. Japanese.

PMID:
1758052
11.

Pseudo Pelger-Huët anomaly in myelodysplastic syndrome: hyposegmented apoptotic neutrophil?

Shetty VT, Mundle SD, Raza A.

Blood. 2001 Aug 15;98(4):1273-5. No abstract available.

12.

[Segmentation disorders of nuclei of neutrophilic granulocytes in the myelodysplasia syndrome].

Berkessy S.

Orv Hetil. 1987 Nov 8;128(45):2365-6. Hungarian. No abstract available.

PMID:
3684253
13.

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.

Clayton P, Fischer B, Mann A, Mansour S, Rossier E, Veen M, Lang C, Baasanjav S, Kieslich M, Brossuleit K, Gravemann S, Schnipper N, Karbasyian M, Demuth I, Zwerger M, Vaya A, Utermann G, Mundlos S, Stricker S, Sperling K, Hoffmann K.

Nucleus. 2010 Jul-Aug;1(4):354-66. doi: 10.4161/nucl.1.4.12435. Epub 2010 May 21.

14.

Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR.

Borovik L, Modaff P, Waterham HR, Krentz AD, Pauli RM.

Am J Med Genet A. 2013 Aug;161A(8):2066-73. doi: 10.1002/ajmg.a.36019. Epub 2013 Jul 3.

PMID:
23824842
15.

The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils.

Cohen TV, Klarmann KD, Sakchaisri K, Cooper JP, Kuhns D, Anver M, Johnson PF, Williams SC, Keller JR, Stewart CL.

Hum Mol Genet. 2008 Oct 1;17(19):2921-33. doi: 10.1093/hmg/ddn191. Epub 2008 Jul 11.

16.

Homozygous form of the Pelger-Huët leukocyte anomaly in man.

Aznar J, Vaya A.

Acta Haematol. 1981;66(1):59-62.

PMID:
6794302
17.

[Pelger-Huët anomaly].

Shinjo K, Ohno R.

Ryoikibetsu Shokogun Shirizu. 2000;(32):139-41. Review. Japanese. No abstract available.

PMID:
11212667
18.

[Pelger-Huët anomaly].

Shinjo K, Ohno R.

Ryoikibetsu Shokogun Shirizu. 1998;(21 Pt 2):53-5. Review. Japanese. No abstract available.

PMID:
9833425
19.

[A case of marked pseudo-Pelger-Huet anomaly of neutrophils in a patient with myelodysplastic syndrome and partial red cell aplasia (a special type of acute leukemia with pathologic blast differentiation)].

Iavorkovskiĭ LL, Sused SG, Amolina AIa, Soloveĭ DIa, Riauzova LIu.

Gematol Transfuziol. 1989 May;34(5):46-9. Russian. No abstract available.

PMID:
2501144
20.

Pelger-Huët anomaly in a cat.

Deshuillers P, Raskin R, Messick J.

Vet Clin Pathol. 2014 Sep;43(3):337-41. doi: 10.1111/vcp.12176. Epub 2014 Aug 12.

PMID:
25115222

Supplemental Content

Support Center