• A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
• A case of loose anagen syndrome in an African American girl
• A case report of Noonan syndrome-like disorder with loose anagen hair 2 treated with recombinant human growth hormone
• A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
• A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair
• A Novel SHOC2 Variant in Rasopathy
• A very mild phenotype in six individuals of a three-generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS-related RASopathy distinct from Costello syndrome
• A very mild phenotype in six individuals of a three-generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS-related RASopathy distinct from Costello syndrome
• Aberrant N-myristoylation as a prelude to autoimmune manifestations in patients with SHOC2 mutations
• ADA2 deficiency in a patient with Noonan syndrome-like disorder with loose anagen hair: The co-occurrence of two rare syndromes
• Alopecia in genetic diseases
• Anagen effluvium
• Anagen Effluvium
• Antenatal diagnosis of cardio-facio-cutaneous syndrome: Prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. About a case and review of literature
• Assessing the gene-disease association of 19 genes with the RASopathies using the ClinGen gene curation framework
• Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
• Behavioral profile in RASopathies
• Cardiomyopathies in Noonan syndrome and the other RASopathies
• Case report: A <em>de novo</em> RASopathy-causing <em>SHOC2</em> variant in a Chinese girl with noonan syndrome-like with loose anagen hair
• Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair
• Case report: Identification and clinical phenotypic analysis of novel mutation of the <em>PPP1CB</em> gene in NSLH2 syndrome
• Case report: Identification and clinical phenotypic analysis of novel mutation of the PPP1CB gene in NSLH2 syndrome
• Central nervous system involvement in individuals with RASopathies
• Cleft palate and hypopituitarism in a patient with Noonan-like syndrome with loose anagen hair-1
• Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy
• Clinical overview on RASopathies
• Co-Occurring Thrombotic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in a Child Carrying the Pathogenic SHOC2 c.4A&gt;G (p.Ser2Gly) Variant
• Coarctation of the aorta in Noonan-like syndrome with loose anagen hair
• Cutaneous T-cell lymphoma in SHOC2 mutation-associated Noonan-like syndrome with loose anagen hair
• Dermatological manifestations, management, and care in RASopathies
• Diagnosis and management of alopecia in children
• Diagnosis of Noonan syndrome and related disorders using target next generation sequencing
• Epilepsy in a cohort of children with Noonan syndrome and related disorders
• Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications
• Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndrome
• Expert consensus on the management of Telogen Effluvium in India
• Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair
• GH Therapy and first final height data in Noonan-like syndrome with loose anagen hair (Mazzanti syndrome)
• Hair loss in children
• Hair pull test: Evidence-based update and revision of guidelines
• Hematopoietic and neural crest defects in zebrafish shoc2 mutants: a novel vertebrate model for Noonan-like syndrome
• Hydrops fetalis in a preterm newborn heterozygous for the c.4A&gt;G SHOC2 mutation
• Improved growth velocity of a patient with Noonan-like syndrome with loose anagen hair (NS/LAH) without growth hormone deficiency by low-dose growth hormone therapy
• Light microscopic hair abnormalities in children: retrospective review of 119 cases in a 10-year period
• Loose anagen hair syndrome
• Loose Anagen Hair Syndrome
• Loose Anagen Hair Syndrome
• Loose Anagen Hair Syndrome in a Saudi Girl
• Loose anagen hair syndrome: Is there any association with atopic dermatitis?
• Loose anagen hair syndrome: take a closer look!
• Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
• Loose Anagen Syndrome
• Loose Anagen Syndrome
• Loose anagen syndrome in one identical twin girl
• Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
• Low-dose oral minoxidil improves global hair density and length in children with loose anagen hair syndrome
• M-type phospholipase A2 receptor-associated membranous nephropathy in a patient with Noonan-like syndrome with loose anagen hair
• Minoxidil 5% solution for topical treatment of loose anagen hair syndrome
• Monogenic systemic lupus erythematosus onset in a 13-year-old boy with Noonan like-syndrome: a case report and literature review
• Morroniside regulates hair growth and cycle transition via activation of the Wnt/beta-catenin signaling pathway
• Morroniside regulates hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway
• Moyamoya disease in two patients with Noonan-like syndrome with loose anagen hair
• Moyamoya syndrome in a patient with Noonan-like syndrome with loose anagen hair
• Mutation and Phenotypic Spectrum of Patients With RASopathies
• N(1)-methylspermidine, a stable spermidine analog, prolongs anagen and regulates epithelial stem cell functions in human hair follicles
• Natural history and outcomes in paediatric RASopathy-associated hypertrophic cardiomyopathy
• Noonan syndrome - a new survey
• Noonan syndrome and Noonan-like syndrome with loose anagen hair: rare phenotypes may emerge during follow-up
• Noonan syndrome with loose anagen hair associated with trichorrhexis nodosa and trichoptilosis
• Noonan syndrome with loose anagen hair with variants in the PPP1CB gene: First familial case reported
• Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastoma
• Oral minoxidil treatment for hair loss: A review of efficacy and safety
• Paternal isodisomy of chromosome 5 in a patient with recessive multiple epiphyseal dysplasia
• Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp
• Phenotypic variability associated with the invariant SHOC2 c.4A&gt;G (p.Ser2Gly) missense mutation
• PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain
• RASopathies: Dermatologists' viewpoints
• Recurrent Erythema Nodosum in a Child with a <em>SHOC2</em> Gene Mutation
• Review of oral minoxidil as treatment of hair disorders: in search of the perfect dose
• Shoc2 controls ERK1/2-driven neural crest development by balancing components of the extracellular matrix
• SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signalling
• Short anagen hair syndrome
• Short anagen syndrome: A case series and algorithm for diagnosis
• Short anagen syndrome: Case series and literature review
• Systemic lupus erythematosus in a patient with Noonan syndrome-like disorder with loose anagen hair 1: More than a chance association
• The expression of congenital Shoc2 variants induces AKT-dependent crosstalk activation of the ERK1/2 pathway
• The expression of congenital Shoc2 variants induces AKT-dependent feedback activation of the ERK1/2 pathway
• The perinatal presentation of cardiofaciocutaneous syndrome
• The psychologic impact of loose anagen syndrome and short anagen syndrome
• The RASopathies: Biology, genetics and therapeutic options
• The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway
• The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotype
• The role of USP7 in the Shoc2-ERK1/2 signaling axis and Noonan-like syndrome with loose anagen hair
• Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots
• Trichotillomania: Bizzare Patern of Hair Loss at 11-Year-old Girl
• Two Japanese patients with Noonan syndrome-like disorder with loose anagen hair 2
• Uncombable hair syndrome and beyond
• Utility of Teledermatology in the Diagnosis of Loose Anagen Syndrome
• What looks like alopecia areata is not always alopecia areata
• Your patient complains about hair loss. Contribution of a skin biopsy in noncicatricial alopecias