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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Extraintestinal Manifestations of Coeliac Disease
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Prolactinomas
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Anti-Ma and Anti-Ta Associated Paraneoplastic Neurological Syndromes: 22 Newly Diagnosed Patients and Review of Previous Cases
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Sarcoidosis: Clinical, Hormonal, and Magnetic Resonance Imaging (MRI) Manifestations of Hypothalamic-Pituitary Disease in 9 Patients and Review of the Literature
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Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
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Prolactinoma
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Prader-Willi and Angelman Syndromes
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Diagnosis and Management of Pituitary Tumours
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Hypothalamic-Pituitary Dysfunction after Radiation for Brain Tumors
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Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Accelerated Aging of the Brain in Werner's Syndrome
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Cockayne Syndrome: Review of 140 Cases
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X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
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Physical Features of Prader-Willi Syndrome in Neonates
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Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
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Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
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Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
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Isolated CNS Sarcoidosis
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Prolactin-Secreting Tumors & Hypogonadism in 22 Men
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Abnormal Iris Vasculature in Myotonic Dystrophy
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Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
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The Oculopharyngeal Syndrome
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Occipital Condyle Syndrome
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Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
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Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
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Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
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A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
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A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
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Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
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A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
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Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
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