• 12-year-old male with Elejalde syndrome (neuroectodermal melanolysosomal disease)
• A 15-year-old boy with silvery white hair, hepatosplenomegaly, and pancytopenia
• A case of Griscelli syndrome
• A novel RAB27A mutation in a patient with Griscelli syndrome type 2
• A rare pigmentary disorder in two non-identical siblings: Griscelli Syndrome -type 3
• A rare syndrome in the differential diagnosis of hepatosplenomegaly and pancytopenia: report of identical twins with Griscelli disease
• Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl
• Albinism and Primary Immunodeficiency in Infants: A Case Study of Griscelli Syndrome
• arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndrome
• Association of Anti N-methyl-D-aspartate (NMDA) Receptor Encephalitis with Chediak-Higashi Syndrome
• Bilateral basal ganglia involvement in a patient with Griscelli syndrome
• Black hair follicular dysplasia in Large Munsterlander dogs: clinical, histological and ultrastructural features
• Bone marrow transplantation (BMT) for the syndrome of pigmentary dilution and lymphohistiocytosis (Griscelli's syndrome)
• Boy with silvery grey hair and immunodeficiency
• Case series on Silvery Hair Syndromes: Single Center Experience
• Chediak-Higashi Syndrome With Epstein-Barr Virus Triggered Hemophagocytic Lymphohistiocytosis: A Case Report
• Chediak-higashi syndrome: a case report
• Chediak-higashi syndrome: a case report of a girl without silvery hair and oculocutaneous albinism presenting with hemophagocytic lymphohistiocytosis
• Chediak-Higashi Syndrome: A Case Series from Karnataka, India
• Chediak-Higashi syndrome: Lessons from a single-centre case series
• Clinico-hematological profile of Chediak-Higashi syndrome: experience from a tertiary care center in south India
• Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes
• Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2
• Diagnostic and therapeutic caveats in Griscelli syndrome
• Elejalde syndrome - A neuroectodermal melanolysosomal disease: A case report
• Elejalde syndrome (ES)
• Elejalde syndrome--a melanolysosomal neurocutaneous syndrome: clinical and morphological findings in 7 patients
• Elejalde syndrome: clinical and histopathological findings in an Egyptian male
• Elejalde syndrome: report of a case and review of the literature
• Evaluation of hair structural abnormalities in children with different neurological diseases
• Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene
• Griscelli syndrome
• Griscelli syndrome - a case report
• Griscelli syndrome in a Mexican girl
• Griscelli syndrome in Mexico. Description of a case with neurological manifestations
• Griscelli Syndrome in Skin of Color: A Trichoscopic Perspective
• Griscelli syndrome subtype 2 with hemophagocytic lympho-histiocytosis: A case report and review of literature
• Griscelli syndrome type 1: a novel pathogenic variant, and review of literature
• Griscelli syndrome type 2; a pediatric case with immunodeficiency
• Griscelli syndrome type 2: long-term follow-up after unrelated donor bone marrow transplantation
• Griscelli Syndrome Type 3 with Coexistent Universal Dyschromia-An Uncommon Association of a Rare Entity
• Griscelli syndrome type 3: A new case
• Griscelli Syndrome Type 3: Two New Cases and Review of the Literature
• Griscelli syndrome type-3
• Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients
• Griscelli Syndrome With Hemophagocytic Lymphohistiocytosis: A Rare Case Report
• Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: expanding the phenotypic spectrum of Rab27A mutations in humans
• Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure
• Griscelli syndrome: hemophagocytic lymphohistiocytosis with silvery hair
• Griscelli's Syndrome: Clinical and Immunological Features of Two Siblings
• Griscelli's syndrome: clinical features of three siblings
• Haemophagocytic lymphohistiocytosis and silvery hair in Griscelli syndrome
• Hair cross-sectioning in uncombable hair syndrome: An epoxy embedding technique
• Hair Shaft Examination: A Practical Tool to Diagnose Griscelli Syndrome
• Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report
• Light and scanning electron microscopic examination of hair in Griscelli syndrome
• Macrophage activation syndrome associated with griscelli syndrome type 2: case report and review of literature
• Myosin V colocalizes with melanosomes and subcortical actin bundles not associated with stress fibers in human epidermal melanocytes
• Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2
• Oral features of Griscelli syndrome type II: A rare case report
• Partial albinism with immunodeficiency (Griscelli syndrome)
• Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature
• Partial albinism, immunodeficiency, and progressive white matter disease: a new primary immunodeficiency
• Partial albinism, immunodeficiency, hypergammaglobulinemia and Dandy-Walker cyst--a Griscelli syndrome variant
• Pili trianguli et canaliculi: a distinctive hair shaft defect leading to uncombable hair
• Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome
• Rab27 effectors, pleiotropic regulators in secretory pathways
• Rab27b is up-regulated in human Griscelli syndrome type II melanocytes and linked to the actin cytoskeleton via exon F-Myosin Va transcripts
• Rare Challenges in Diagnosing Cushing's Syndrome and Primary Aldosteronism: A Case Report of a Female With a Negative Workup
• Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair
• Roberts-SC phocomelia syndrome: cytogenetic findings and clinical variability in three brothers
• Seizure as the presenting manifestation in Griscelli syndrome type 2
• Severe anemia due to parvovirus B19 in a silver haired boy
• Silvery Gray Hair Syndrome With Hemophagocytic Lymphohistiocytosis: A Case Report
• Silvery Gray Hair: A Clue to Diagnosing Chediak-Higashi Syndrome
• Silvery grey hair: clue to diagnose immunodeficiency
• Silvery hair in children: a symptom of leucogranulocytic and melanocytic diseases (author's transl)
• Silvery hair syndrome in two cousins: Chediak-Higashi syndrome vs Griscelli syndrome, with rare associations
• Silvery hair with bronze-tan in a child: A case of Elejalde disease
• Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis
• Silvery Hair with Speckled Dyspigmentation: Chediak-Higashi Syndrome in Three Indian Siblings
• Silvery-gray hair in a newborn
• Skin manifestations in primary immunodeficient children
• Slivers of Hair - A Clue to Uncover Silver Hair Syndromes
• Spontaneous repigmentation of silvery hair in an infant with congenital hydrops fetalis and hypoproteinemia
• Successful use of emapalumab in refractory hemophagocytic lymphohistiocytosis in a child with Chediak-Higashi syndrome: a case report
• Teaching neuroImages: Griscelli syndrome and CNS lymphohistiocytosis
• The color of skin: gray diseases of the skin, nails, and mucosa
• The GTPase-deficient Rab27A(Q78L) mutant inhibits melanosome transport in melanocytes through trapping of Rab27A effector protein Slac2-a/melanophilin in their cytosol: development of a novel melanosome-targetinG tag
• Two novel mutations identified in an african-american child with chediak-higashi syndrome
• Usefulness of the skin biopsy as a tool in the diagnosis of silvery hair syndrome
• Versatile role of Rab27 in membrane trafficking: focus on the Rab27 effector families
• Whole-Exome Sequencing, Proteome Landscape, and Immune Cell Migration Patterns in a Clinical Context of Menkes Disease