| This article has been cited by |
| 1 | Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing | |
| Adel M. Abuzenadah,Galila F. Zaher,Ashraf Dallol,Ghazi A. Damanhouri,Adeel G. Chaudhary,Faten Al-Sayes,Mamdooh A. Gari,Mofareh AlZahrani,Salwa Hindawi,Mohammed H. Al-Qahtani |
| Journal of Thrombosis and Thrombolysis.2013;36(4)501 |
| [DOI] |
|
| 2 | Common Variable Immunodeficiency Associated with Partial Albinism | |
| Suneel Mundkur,Sandeep Kumar,Shrikiran Aroor |
| Pediatric Oncall.2015;12(2)501 |
| [DOI] |
|
| 3 | Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis | |
| Meenakshi Batrani,Akhilesh Thole,Asha Kubba,Khushbu Mahajan |
| Journal of Cutaneous Pathology.2018;45(12)918 |
| [DOI] |
|
| 4 | Hair greying & its palliative management | |
| Sunil Chaudhry |
| Southeast Asian Journal of Health Professional.2022;5(3)58 |
| [DOI] |
|
| 5 | Hair greying & its palliative management | |
| Chao-Chun Yang,Chih-Chiang Chen,Wen-Chieh Chen |
| Southeast Asian Journal of Health Professional.2014;5(3)231 |
| [DOI] |
|
| 6 | The color of skin: gray diseases of the skin, nails, and mucosa | |
| M. Badawy Abdel-Naser |
| Clinics in Dermatology.2019;37(5)507 |
| [DOI] |
|
| 7 | A new
NOTCH3
damaging variant in a thrombocytopenia family of Miao ethnic group | |
| Yingling Zhao,Juheng Li |
| The Journal of Gene Medicine.2019;21(11)507 |
| [DOI] |
|
| 8 | Griscelli syndrome Type 2: A report of rare case | |
| Chandramohan Kudligi,PradeepVittal Bhagwat,MaryZothanpuii Chhangte,Vidya Kuntoji,Sujata Giriyan,Veena Andanappanavar |
| Clinical Dermatology Review.2017;1(2)65 |
| [DOI] |
|
| 9 | A Girl with Gray Hair and Pyogenic Infections | |
| Sara Palencia-Pérez,Fátima Tous-Romero,Ana María Delgado-Márquez |
| Pediatric Dermatology.2017;34(5)607 |
| [DOI] |
|
| 10 | Hemiparesis Revealing a Unique Neurological Hemophagocytic Lymphohistiocytosis in a Patient With Griscelli Syndrome Type 2 | |
| Othman Moueqqit,Ghanam Ayad,Madiha Benhachem,Abdelilah Lahmar,Hiba Ramdani,Miry Nadir,Mohammed Bensalah,Amal Bennani,Imane Kamaoui,Rachid Seddik,Noufissa Benajiba |
| Cureus.2022;34(5)607 |
| [DOI] |
|
| 11 | Cutaneous presentation in chediak – Higashi syndrome – A rare case report | |
| Zebasultana Saiyed,Shilpa Singh,Vardendra Kulkarni |
| IP Archives of Cytology and Histopathology Research.2022;7(4)251 |
| [DOI] |
|
| 12 | Allogeneic hematopoietic stem cell transplant in rare hematologic disorders: a single center experience from Pakistan | |
| Maryam Khan,Raheel Iftikhar,Tariq Ghafoor,Fayyaz Hussain,Qamar un Nisa Chaudhry,Syed Kamran Mahmood,Nighat Shahbaz,Mehreen Ali Khan,Tariq Azam Khattak,Ghassan Umair Shamshad,Jahanzeb Rehman,Sundas Ali,Zunaira Shah,Abdul Rafae,Muhammad Farhan,Faiz Anwer,Parvez Ahmed |
| Bone Marrow Transplantation.2021;56(4)863 |
| [DOI] |
|
| 13 | Hair Shaft Examination: A Practical Tool to Diagnose Griscelli Syndrome | |
| Trinidad Montero-Vilchez,Alexandra Remon-Love,Jesús Tercedor-Sánchez,Salvador Arias-Santiago |
| Dermatopathology.2021;8(1)49 |
| [DOI] |
|
| 14 | Ophthalmological Manifestations of Oculocutaneous and Ocular Albinism: Current Perspectives | |
| Magella M Neveu,Srikanta Kumar Padhy,Srishti Ramamurthy,Brijesh Takkar,Subhadra Jalali,Deepika CP,Tapas Ranjan Padhi,Anthony G Robson |
| Clinical Ophthalmology.2022;Volume 16(1)1569 |
| [DOI] |
|
| 15 | Griscelli Syndrome in a seven years old girl | |
| Borhan Moradveisi,Avat Karimi,Shirin Behzadi,Farima Zakaryaei |
| Clinical Case Reports.2021;9(5)1569 |
| [DOI] |
|
| 16 | Síndrome de Chediak-Higashi: microscopia óptica del pelo | |
| G. Blasco-Morente,C. Garrido-Colmenero,J. Aneiros-Fernández,J. Tercedor-Sánchez |
| Anales de Pediatría.2016;84(1)62 |
| [DOI] |
|
