Similar articles for PMID: 1595481

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Partial albinism with immunodeficiency: a rare syndrome with prominent posterior fossa white matter changes.

Brismar J, Harfi HA. Brismar J, et al. AJNR Am J Neuroradiol. 1992 Jan-Feb;13(1):387-93. AJNR Am J Neuroradiol. 1992. PMID: 1595481

Griscelli syndrome type 2: A rare and fatal syndrome in a South Indian boy.

Rajyalakshmi R, Chakrapani RN. Rajyalakshmi R, et al. Indian J Pathol Microbiol. 2016 Jan-Mar;59(1):113-6. doi: 10.4103/0377-4929.178230. Indian J Pathol Microbiol. 2016. PMID: 26960655 Free article.

Neurological presentation of Griscelli syndrome: obstructive hydrocephalus without haematological abnormalities or organomegaly.

Rajadhyax M, Neti G, Crow Y, Tyagi A. Rajadhyax M, et al. Brain Dev. 2007 May;29(4):247-50. doi: 10.1016/j.braindev.2006.09.007. Epub 2006 Nov 7. Brain Dev. 2007. PMID: 17085000

Neuroimaging abnormalities in Griscelli's disease.

Sarper N, Akansel G, Aydoğan M, Gedikbaşi D, Babaoğlu K, Gökalp AS. Sarper N, et al. Pediatr Radiol. 2002 Dec;32(12):875-8. doi: 10.1007/s00247-002-0752-1. Epub 2002 Jul 17. Pediatr Radiol. 2002. PMID: 12447595

Haemophagocytic lymphohistiocytosis and silvery hair in Griscelli syndrome.

Lipsker D. Lipsker D. Br J Haematol. 2016 Oct;175(1):11. doi: 10.1111/bjh.14252. Epub 2016 Jul 19. Br J Haematol. 2016. PMID: 27434021 No abstract available.

[Griscelli syndrome].

Svenningsen P, Petersen BL, Ryder LP, Broholm H, Møller-Hansen KJ, Glenthøj JP, Heilmann CJ, Müller KG. Svenningsen P, et al. Ugeskr Laeger. 2004 Feb 9;166(7):600-2. Ugeskr Laeger. 2004. PMID: 15005046 Danish. No abstract available.

PARTIAL OCULOCUTANEOUS ALBINISM AND IMMUNODEFICIENCY SYNDROMES: TEN YEARS EXPERIENCE FROM A SINGLE CENTER IN TURKEY.

Patiroglu T, Akar HH, Unal E, Chiang SC, Schlums H, Tesi B, Ozkars MY, Karakukcu M. Patiroglu T, et al. Genet Couns. 2016;27(1):67-76. Genet Couns. 2016. PMID: 27192893

MR imaging of white matter disease in children.

Nowell MA, Grossman RI, Hackney DB, Zimmerman RA, Goldberg HI, Bilaniuk LT. Nowell MA, et al. AJR Am J Roentgenol. 1988 Aug;151(2):359-65. doi: 10.2214/ajr.151.2.359. AJR Am J Roentgenol. 1988. PMID: 3260728

Griscelli syndrome: Rab 27a mutation.

Sheela SR, Latha M, Injody SJ. Sheela SR, et al. Indian Pediatr. 2004 Sep;41(9):944-7. Indian Pediatr. 2004. PMID: 15475639 Free article.

Partial albinism, immunodeficiency, and progressive white matter disease: a new primary immunodeficiency.

Harfi HA, Brismar J, Hainau B, Sabbah R. Harfi HA, et al. Allergy Proc. 1992 Nov-Dec;13(6):321-8. doi: 10.2500/108854192778816933. Allergy Proc. 1992. PMID: 1490625

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