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Items: 1 to 20 of 40

1.

Griscelli Syndrome Type 3: Two New Cases and Review of the Literature.

Nouriel A, Zisquit J, Helfand AM, Anikster Y, Greenberger S.

Pediatr Dermatol. 2015 Nov-Dec;32(6):e245-8. doi: 10.1111/pde.12663. Review.

PMID:
26337734
2.

Seizure as the presenting manifestation in Griscelli syndrome type 2.

Panigrahi I, Suthar R, Rawat A, Behera B.

Pediatr Neurol. 2015 May;52(5):535-8. doi: 10.1016/j.pediatrneurol.2015.01.010.

PMID:
25801174
3.

Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2).

Henkes M, Finke J, Warnatz K, Ammann S, Stadt UZ, Janka G, Brugger W.

Ann Hematol. 2015 Jun;94(6):1057-60. doi: 10.1007/s00277-014-2284-9. No abstract available.

PMID:
25544030
4.

A case of Griscelli syndrome.

Kerketta JA, Lodh M, Mandal K.

Dermatol Online J. 2014 Nov 15;20(11). pii: 13030/qt96f7z0gw.

PMID:
25419745
5.

Cerebellar involvement of Griscelli syndrome type 2.

Işikay S.

BMJ Case Rep. 2014 Oct 14;2014. pii: bcr2014206703. doi: 10.1136/bcr-2014-206703.

6.

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding.

Cetica V, Hackmann Y, Grieve S, Sieni E, Ciambotti B, Coniglio ML, Pende D, Gilmour K, Romagnoli P, Griffiths GM, Aricò M.

J Allergy Clin Immunol. 2015 May;135(5):1310-8.e1. doi: 10.1016/j.jaci.2014.08.039.

7.

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.

Yılmaz M, Çağdaş D, Grandin V, Altıntaş DU, Tezcan İ, de Saint Basile G, Sanal Ö.

Pediatr Allergy Immunol. 2014 Dec;25(8):817-9. doi: 10.1111/pai.12285. No abstract available.

PMID:
25283056
8.

A rare pigmentary disorder in two non-identical siblings: Griscelli Syndrome -type 3.

Kaur S, Jindal N, Dayal S, Jain VK, Jairath V, Virdi S.

Dermatol Online J. 2014 Jul 15;20(7). pii: 13030/qt4r42t43w.

9.

Teaching neuroImages: Griscelli syndrome and CNS lymphohistiocytosis.

Saini AG, Nagaraju S, Sahu JK, Rawat A, Vyas S, Singhi P.

Neurology. 2014 Apr 8;82(14):e122-3. doi: 10.1212/WNL.0000000000000288.

PMID:
24711539
10.

Hematopoietic stem cell transplantation with a reduced-intensity conditioning regimen in pediatric patients with Griscelli syndrome type 2.

Hamidieh AA, Pourpak Z, Yari K, Fazlollahi MR, Hashemi S, Behfar M, Moin M, Ghavamzadeh A.

Pediatr Transplant. 2013 Aug;17(5):487-91. doi: 10.1111/petr.12092.

PMID:
23714271
11.

Griscelli syndrome associated with hemophagocytic lymphohistiocytosis.

Love PB, Patterson SS, Prose NS, Atwater AR.

J Drugs Dermatol. 2012 Sep;11(9):1126. No abstract available.

PMID:
23135662
12.

Molecular analysis and clinical findings of Griscelli syndrome patients.

Durmaz A, Ozkinay F, Onay H, Tombuloglu M, Atay A, Gursel O, Peker E, Atmaca M, Genel F, Bozabali S, Akin H, Ozkinay C.

J Pediatr Hematol Oncol. 2012 Oct;34(7):541-4.

PMID:
22983416
13.

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

Cağdaş D, Ozgür TT, Asal GT, Tezcan I, Metin A, Lambert N, de Saint Basile G, Sanal O.

Eur J Pediatr. 2012 Oct;171(10):1527-31.

PMID:
22711375
14.

Pulmonary lymphomatoid granulomatosis in Griscelli syndrome type 2.

Szczawinska-Poplonyk A, Kycler Z, Breborowicz A, Klaudel-Dreszler M, Pac M, Zegadlo-Mylik M, Langfort R.

Viral Immunol. 2011 Dec;24(6):471-3. doi: 10.1089/vim.2011.0034.

PMID:
22111599
15.

Cellular and clinical report of new Griscelli syndrome type III cases.

Westbroek W, Klar A, Cullinane AR, Ziegler SG, Hurvitz H, Ganem A, Wilson K, Dorward H, Huizing M, Tamimi H, Vainshtein I, Berkun Y, Lavie M, Gahl WA, Anikster Y.

Pigment Cell Melanoma Res. 2012 Jan;25(1):47-56. doi: 10.1111/j.1755-148X.2011.00901.x.

16.

A novel RAB27A mutation in a patient with Griscelli syndrome type 2.

Shamsian BS, Norbakhsh K, Rezaei N, Safari A, Gharib A, Pourpak Z, Alavi S, Parvaneh N, Arzanian MT.

J Investig Allergol Clin Immunol. 2010;20(7):612-5.

17.

Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome.

Al-Idrissi E, ElGhazali G, Alzahrani M, Ménasché G, Pachlopnik Schmid J, Basile Gde S.

J Pediatr Hematol Oncol. 2010 Aug;32(6):494-6. doi: 10.1097/MPH.0b013e3181e34dc9. Erratum in: J Pediatr Hematol Oncol. 2011 May;33(4):319.

PMID:
20661159
18.

Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2.

Vincent LM, Gilbert F, DiPace JI, Ciccone C, Markello TC, Jeong A, Dorward H, Westbroek W, Gahl WA, Bussel JB, Huizing M.

Mol Genet Metab. 2010 Sep;101(1):62-5. doi: 10.1016/j.ymgme.2010.05.015.

19.

Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2.

Ohbayashi N, Mamishi S, Ishibashi K, Maruta Y, Pourakbari B, Tamizifar B, Mohammadpour M, Fukuda M, Parvaneh N.

Pigment Cell Melanoma Res. 2010 Jun;23(3):365-74. doi: 10.1111/j.1755-148X.2010.00705.x.

PMID:
20370853
20.

Hematopoietic SCT in children with Griscelli syndrome: a single-center experience.

Al-Ahmari A, Al-Ghonaium A, Al-Mansoori M, Hawwari A, Eldali A, Ayas M, Al-Mousa H, Al-Jefri A, Al-Saud B, Al-Seraihy A, Al-Muhsen S, Al-Mahr M, Al-Dhekri H, El-Solh H.

Bone Marrow Transplant. 2010 Aug;45(8):1294-9. doi: 10.1038/bmt.2009.358.

PMID:
20062095
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