Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 97

Similar articles for PubMed (Select 23888244)

1.

A case report of acute myeloid leukemia and neurofibromatosis 1.

Sartor C, Papayannidis C, Chiara Abbenante M, Curti A, Polverelli N, Ottaviani E, Iacobucci I, Guadagnuolo V, Martinelli G.

Hematol Rep. 2013 Jul 3;5(2):28-9. doi: 10.4081/hr.2013.e8. Print 2013 Jun 28.

2.

Central nervous system lymphoma occurring in a patient with neurofibromatosis type 1 (von Recklinghausen disease).

Eoli M, Bianchessi D, Di Stefano AL, Prodi E, Anghileri E, Finocchiaro G.

Neurol Sci. 2012 Dec;33(6):1429-33. Review.

PMID:
22294052
3.

Patterns of hematopoietic lineage involvement in children with neurofibromatosis type 1 and malignant myeloid disorders.

Miles DK, Freedman MH, Stephens K, Pallavicini M, Sievers EL, Weaver M, Grunberger T, Thompson P, Shannon KM.

Blood. 1996 Dec 1;88(11):4314-20.

4.

Von Recklinghausen neurofibromatosis and hematologic malignancies: 2 case reports in adulthood.

Van Baren N, Issa A, Delannoy A.

Acta Clin Belg. 1993;48(3):164-70. Review.

PMID:
8396298
5.

Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders.

Side L, Taylor B, Cayouette M, Conner E, Thompson P, Luce M, Shannon K.

N Engl J Med. 1997 Jun 12;336(24):1713-20.

6.

Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia.

Boudry-Labis E, Roche-Lestienne C, Nibourel O, Boissel N, Terre C, Perot C, Eclache V, Gachard N, Tigaud I, Plessis G, Cuccuini W, Geffroy S, Villenet C, Figeac M, Leprêtre F, Renneville A, Cheok M, Soulier J, Dombret H, Preudhomme C; French ALFA group.

Am J Hematol. 2013 Apr;88(4):306-11. doi: 10.1002/ajh.23403. Epub 2013 Mar 5.

PMID:
23460398
7.

Von Recklinghausen neurofibromatosis and acute leukemia.

Reich SD, Wiernik PH.

Am J Dis Child. 1976 Aug;130(8):888-9.

PMID:
821339
9.
10.
12.

Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1.

Maris JM, Wiersma SR, Mahgoub N, Thompson P, Geyer RJ, Hurwitz CG, Lange BJ, Shannon KM.

Cancer. 1997 Apr 1;79(7):1438-46.

PMID:
9083167
13.

Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1.

Petrak B, Bendova S, Seeman T, Klein T, Lisy J, Zatrapa T, Marikova T.

Neuro Endocrinol Lett. 2007 Dec;28(6):734-8.

PMID:
18063929
14.

Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genes.

Ercolino T, Lai R, Giachè V, Melchionda S, Carella M, Delitala A, Mannelli M, Fanciulli G.

Gene. 2014 Feb 25;536(2):332-5. doi: 10.1016/j.gene.2013.12.003. Epub 2013 Dec 21.

PMID:
24361808
15.

Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?

Alkindy A, Chuzhanova N, Kini U, Cooper DN, Upadhyaya M.

Hum Genomics. 2012 Aug 13;6:12. doi: 10.1186/1479-7364-6-12.

16.

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.

Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, Farmer GE, Freiman RN, Lee JK, Li FP, et al.

Proc Natl Acad Sci U S A. 1990 Jul;87(14):5435-9.

17.

p53 mutation as the second event in juvenile chronic myelogenous leukemia in a patient with neurofibromatosis type 1.

Luria D, Avigad S, Cohen IJ, Stark B, Weitz R, Zaizov R.

Cancer. 1997 Nov 15;80(10):2013-8.

PMID:
9366306
18.

Incidental finding of isolated colonic neurofibroma.

Chelimilla H, Chandrala CK, Niazi M, Kumbum K.

Case Rep Gastroenterol. 2013 Sep 5;7(3):369-75. doi: 10.1159/000355163. eCollection 2013.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk