• <em>ANOS1</em> variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism
• <em>NOS1</em> mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice
• A case of congenital anosmia
• A Case of Unilateral Proptosis Secondary to Prostatic Metastasis
• A central mechanism of analgesia in mice and humans lacking the sodium channel Na_V1.7
• A Molecular Analysis of Neural Olfactory Placode Differentiation in Human Pluripotent Stem Cells
• A Novel <em>FGFR1</em> Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism
• A novel FGF8 mutation in a female patient with isolated congenital anosmia
• A Novel p.Tyr129His Variant in <em>SIX1</em> Leads to Dominant, Delayed-onset Hearing Loss with Possible Association with Congenital Anosmia
• A Novel p.Tyr129His Variant in SIX1 Leads to Dominant, Delayed-onset Hearing Loss with Possible Association with Congenital Anosmia
• A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism
• A role for TENM1 mutations in congenital general anosmia
• A systematic review of olfactory-related brain structural changes in patients with congenital or acquired anosmia
• A world without the olfactory dimension
• Acute lymphoblastic leukemia in a child with Weiss-Kruszka syndrome: Casual or causal association?
• Advancements in the research of congenital anosmia
• An Extremely Rare Cause of Isolated Congenital Anosmia
• An Indonesian male with congenital hypogonadotropic hypogonadism: A case report and literature review
• Analysis of a patient with Kallmann syndrome and a 45,X/46,XY karyotype
• Analysis of clinical characteristics in the patient with olfactory disorders
• Anosmia
• Anterior Skull Base Abnormalities in Congenital Anosmia
• Bilateral olfactory aplasia: Uncommon cause of congenital anosmia
• Bosma Arhinia Microphthalmia Syndrome (BAMS): First Report from Vietnam
• Brain structure is changed in congenital anosmia
• Clinical and magnetic resonance imaging characteristics of isolated congenital anosmia
• Clinical and MRI Findings in Patients with Congenital Anosmia
• Clinical features of olfactory disorders in patients seeking medical consultation
• Clinical observation of isolated congenital anosmia
• Clinical research of patients with congenital anosmia
• Complex rhinobronchial dystrophy and immunodeficiency: Chance association or exceptional congenital syndrome?
• Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
• Congenital Agenesis of the Olfactory Bulbs: What to Suspect?
• Congenital anosmia and emotion recognition: A case-control study
• Congenital Anosmia and Facial Emotion Recognition
• Congenital anosmia: our experience of eleven patients with aplasia or hypoplasia of the olfactory tract
• Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome
• Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With <em>SMCHD1</em> Variants
• Development of an International Odor Identification Test for Children: The Universal Sniff Test
• Diagnosis and clinical characteristics of congenital anosmia: case series report
• Diagnosis and genetic analysis of a case of Waardenburg syndrome type 2 with hypogonadotropic hypogonadism caused by <em>SOX10</em> gene deletion
• Diagnosis of isolated congenital anosmia using simultaneous functional magnetic resonance imaging and olfactory event-related potentials: Our experience in six patients
• Etiologies of olfactory dysfunction in a pediatric population: based on a retrospective analysis of data from an outpatient clinic
• GNRHR-related central hypogonadism with spontaneous recovery - case report
• Gray matter alteration in isolated congenital anosmia patient: a voxel-based morphometry study
• How to measure olfactory bulb volume and olfactory sulcus depth?
• Identification of a novel mutation in <em>FGFR1</em> gene in mother and daughter with Kallmann syndrome
• Identifying candidate genes underlying isolated congenital anosmia
• Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a Nose
• Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes
• Investigating morphological changes in the brain in relation to etiology and duration of olfactory dysfunction with voxel-based morphometry
• Is congenital anosmia protective for Parkinson's disease triggered by pathogenic entrance through the nose?
• Isolated and syndromic forms of congenital anosmia
• Isolated Congenital Anosmia and CNGA2 Mutation
• Isolated congenital anosmia--clinical and daily life aspects of a life without a sense of smell
• Isolated Congenital Anosmia: Case Report and Literature Review
• Kallmann Syndrome
• Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia
• Learning about the functions of the olfactory system from people without a sense of smell
• Lifelong olfactory deprivation-dependent cortical reorganization restricted to orbitofrontal cortex
• Long COVID syndrome after SARS-CoV-2 survival in patients with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension
• Machine-learned pattern identification in olfactory subtest results
• Making sense of the chemical senses
• Matters Arising: Is congenital anosmia protective for Parkinson's disease triggered by pathogenic entrance through the nose?
• Men without a sense of smell exhibit a strongly reduced number of sexual relationships, women exhibit reduced partnership security - a reanalysis of previously published data
• Morphological changes in secondary, but not primary, sensory cortex in individuals with life-long olfactory sensory deprivation
• Nasal Construction in Congenital Arhinia Due to Novel SMCHD1 Gene Variant
• Neural processing of olfactory-related words in subjects with congenital and acquired olfactory dysfunction
• New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism
• Next-generation sequencing of patients with congenital anosmia
• Normal Olfactory Functional Connectivity Despite Lifelong Absence of Olfactory Experiences
• Novel <em>PAX6</em> variant in a family with ophthalmologic, pancreatic, and olfactory features
• Novel SCN9A variant associated with congenital insensitivity to pain
• Olfaction in the autism spectrum
• Olfactory dysfunction affects thresholds to trigeminal chemosensory sensations
• Olfactory function and olfactory bulbs in patients with Kallmann syndrome
• Olfactory Loss and Regain: Lessons for Neuroplasticity
• Olfactory Radioanatomical Findings in Patients With Cardiac Arrhythmias, COVID-19, and Healthy Controls
• Pediatric anosmia: A case series
• PROKR2 and PROK2 mutations cause isolated congenital anosmia without gonadotropic deficiency
• qU-Sniff - the development of a short version of the Universal "Sniffin' Sticks" test
• Radiological findings in congenital anosmia: a case report
• Reply to Matters Arising: Is congenital anosmia protective for Parkinson's disease triggered by pathogenic entrance through the nose?
• SCN9A-associated congenital insensitivity to pain and anosmia in an Irish patient
• Seeing Beyond Your Nose? The Effects of Lifelong Olfactory Sensory Deprivation on Cerebral Audio-visual Integration
• Study on the clinical characteristics of isolated congenital anosmia
• Subjects with congenital anosmia have larger peripheral but similar central trigeminal responses
• Subtle Differences in Brain Architecture in Patients with Congenital Anosmia
• Successful pregnancy and delivery after a vitrified-warmed embryo transfer in a woman with Kallmann syndrome: A case report and literature review
• Taste perception in kallmann syndrome, a model of congenital anosmia
• The clinical significance of electrophysiological measures of olfactory function
• The depth of the olfactory sulcus is an indicator of congenital anosmia
• The first mutation in CNGA2 in two brothers with anosmia
• The Olfactory Nerve: Anatomy and Pathology
• The prevalence of symptoms and its correlation with sex in polish COVID-19 adult patients: Cross-sectional online open survey
• The use of MRI in a tertiary smell and taste clinic: Lessons learned based on a retrospective analysis
• Treatment of congenital hypogonadotropic hypogonadism in male patients
• TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy
• Two Sisters with Kallmann Syndrome, Gonadal Dysgenesis, and Multiple Neuromuscular and Endocrine Disorders: Report of Two Cases with Description of an Unusual Association
• When anorexia nervosa symptoms mask Kallmann syndrome