Boon LM - Search Results

1

Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect.

Brouillard P, Ghassibé M, Penington A, Boon LM, Dompmartin A, Temple IK, Cordisco M, Adams D, Piette F, Harper JI, Syed S, Boralevi F, Taïeb A, Danda S, Baselga E, Enjolras O, Mulliken JB, Vikkula M. Brouillard P, et al. Among authors: boon lm. J Med Genet. 2005 Feb;42(2):e13. doi: 10.1136/jmg.2004.024174. J Med Genet. 2005. PMID: 15689436 Free PMC article.

2

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Gallione CJ, Pasyk KA, Boon LM, Lennon F, Johnson DW, Helmbold EA, Markel DS, Vikkula M, Mulliken JB, Warman ML, et al. Gallione CJ, et al. Among authors: boon lm. J Med Genet. 1995 Mar;32(3):197-9. doi: 10.1136/jmg.32.3.197. J Med Genet. 1995. PMID: 7783168 Free PMC article.

3

Not all hemangiomas look like strawberries: uncommon presentations of the most common tumor of infancy.

Martinez-Perez D, Fein NA, Boon LM, Mulliken JB. Martinez-Perez D, et al. Among authors: boon lm. Pediatr Dermatol. 1995 Mar;12(1):1-6. doi: 10.1111/j.1525-1470.1995.tb00114.x. Pediatr Dermatol. 1995. PMID: 7792211

4

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML. Boon LM, et al. Hum Mol Genet. 1994 Sep;3(9):1583-7. doi: 10.1093/hmg/3.9.1583. Hum Mol Genet. 1994. PMID: 7833915

5

Congenital fibrosarcoma masquerading as congenital hemangioma: report of two cases.

Boon LM, Fishman SJ, Lund DP, Mulliken JB. Boon LM, et al. J Pediatr Surg. 1995 Sep;30(9):1378-81. doi: 10.1016/0022-3468(95)90514-6. J Pediatr Surg. 1995. PMID: 8523253

6

Congenital hemangioma: evidence of accelerated involution.

Boon LM, Enjolras O, Mulliken JB. Boon LM, et al. J Pediatr. 1996 Mar;128(3):329-35. doi: 10.1016/s0022-3476(96)70276-7. J Pediatr. 1996. PMID: 8774499

7

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

Vikkula M, Boon LM, Carraway KL 3rd, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR. Vikkula M, et al. Among authors: boon lm. Cell. 1996 Dec 27;87(7):1181-90. doi: 10.1016/s0092-8674(00)81814-0. Cell. 1996. PMID: 8980225 Free article.

8

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Boon LM, Brouillard P, Irrthum A, Karttunen L, Warman ML, Rudolph R, Mulliken JB, Olsen BR, Vikkula M. Boon LM, et al. Am J Hum Genet. 1999 Jul;65(1):125-33. doi: 10.1086/302450. Am J Hum Genet. 1999. PMID: 10364524 Free PMC article.

9

Complications of systemic corticosteroid therapy for problematic hemangioma.

Boon LM, MacDonald DM, Mulliken JB. Boon LM, et al. Plast Reconstr Surg. 1999 Nov;104(6):1616-23. doi: 10.1097/00006534-199911000-00002. Plast Reconstr Surg. 1999. PMID: 10541160

10

KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation.

Eerola I, Plate KH, Spiegel R, Boon LM, Mulliken JB, Vikkula M. Eerola I, et al. Among authors: boon lm. Hum Mol Genet. 2000 May 22;9(9):1351-5. doi: 10.1093/hmg/9.9.1351. Hum Mol Genet. 2000. PMID: 10814716

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