• <em>MYO5A</em> Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1
• Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes
• Development, characterization, and hematopoietic differentiation of Griscelli syndrome type 2 induced pluripotent stem cells
• Diagnostic and therapeutic caveats in Griscelli syndrome
• Further evidence for genotype-phenotype disparity in Griscelli syndrome
• Genetic analysis in three Egyptian patients with Griscelli syndrome Type 1 reveals new nonsense mutations in MYO5A
• Griscelli syndrome type 1: a novel pathogenic variant, and review of literature
• Griscelli Syndrome Type 1: Hair Microscopy Clinches the Diagnosis
• Griscelli Syndrome Type 3 in Siblings
• Griscelli syndrome: A rare disorder
• Hematopoietic stem cell transplantation for children with primary immunodeficiency diseases: single center experience in Jordan
• Hemiparesis Revealing a Unique Neurological Hemophagocytic Lymphohistiocytosis in a Patient With Griscelli Syndrome Type 2
• High Prevalence of Hemophagocytic Lymphohistiocytosis in Acute Liver Failure of Infancy
• Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (<em>FBP1, ACAD9)</em> and vesicle trafficking <em>(RAB27A)</em>
• Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient
• MYO5A Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1
• Myosin Va and spermine synthase: partners in exosome transport
• Neonatal Onset of Hemophagocytic Lymphohistiocytosis Due to Prenatal Varicella-Zoster Infection in a Neonate with Griscelli Syndrome Type 2
• Optimization of cerebellar purkinje neuron cultures and development of a plasmid-based method for purkinje neuron-specific, miRNA-mediated protein knockdown
• Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals
• Prolonged SARS-CoV-2 RNA virus shedding and lymphopenia are hallmarks of COVID-19 in cancer patients with poor prognosis
• Rubella vaccine-induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity
• Slivers of Hair - A Clue to Uncover Silver Hair Syndromes
• Successful rescue of a lethal Griscelli syndrome type 2 presenting with neurological involvement and hemophagocytic lymphohistiocytosis: a case report
• Successful treatment of severe myasthenia gravis developed after allogeneic hematopoietic stem cell transplantation with plasma exchange and rituximab
• Teaching neuroImages: Griscelli syndrome and CNS lymphohistiocytosis
• The Polarity and Specificity of Antiviral T Lymphocyte Responses Determine Susceptibility to SARS-CoV-2 Infection in Patients with Cancer and Healthy Individuals
• Usefulness of the skin biopsy as a tool in the diagnosis of silvery hair syndrome