| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1048469985 |
| P356 | DOI | 10.1007/S00408-006-0053-9 |
| P698 | PubMed publication ID | 17294338 |
| P5875 | ResearchGate publication ID | 6511574 |
| P2093 | author name string | Loutfi S. Aboussouan | |
| Michael E. Shy | |||
| Richard A. Lewis | |||
| P2860 | cites work | "Burning feet" as the only manifestation of dominantly inherited sensory neuropathy | Q70906367 |
| [Respiratory disorders in type-1 hereditary motor and sensory neuropathy] | Q71888679 | ||
| Spinal deformity in Charcot-Marie-Tooth disease | Q72056890 | ||
| The safety of flexible endoscopic evaluation of swallowing with sensory testing (FEESST): an analysis of 500 consecutive evaluations | Q73264129 | ||
| Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients | Q73594488 | ||
| Familial bilateral vocal cord paralysis and Charcot-Marie-tooth disease type II-C | Q73632079 | ||
| Neuropathic spinal arthropathy in Charcot-Marie-Tooth disease. A case report | Q73647399 | ||
| Hypertrophic neuropathy: atypical appearances resulting from the combination of type I hereditary motor and sensory neuropathy and diabetes mellitus | Q73687150 | ||
| Phrenic nerve conduction study in demyelinating neuropathies and open-heart surgery | Q73765236 | ||
| Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus | Q74503326 | ||
| Charcot-Marie-Tooth disease type 2 with restless legs syndrome | Q74670905 | ||
| Laryngeal electromyographic findings in Charcot-Marie-Tooth disease type II | Q77997971 | ||
| Clinical indications for noninvasive positive pressure ventilation in chronic respiratory failure due to restrictive lung disease, COPD, and nocturnal hypoventilation--a consensus conference report | Q78147685 | ||
| [A case of Charcot-Marie-Tooth disease (CMT) type 1 complicated by diabetes mellitus (DM) showing bilateral phrenic nerve palsy] | Q78865754 | ||
| Charcot-Marie-Tooth disease type 1A: clinicopathological correlations in 24 patients | Q81385529 | ||
| Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene | Q28250239 | ||
| Diaphragmatic weakness in hereditary motor and sensory neuropathy | Q33588865 | ||
| Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis. | Q34044153 | ||
| Vocal fold paresis of Charcot-Marie-Tooth disease | Q34442995 | ||
| Restless legs syndrome: clinicoetiologic correlates | Q34736912 | ||
| Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33. | Q35451119 | ||
| Charcot-Marie-Tooth disease: an update | Q35887723 | ||
| Apathy and hypersomnia are common features of myotonic dystrophy | Q36318043 | ||
| Measurement of lung volumes. | Q38649190 | ||
| Subclinical sensory neuropathy in late-onset restless legs syndrome | Q39424951 | ||
| Mechanics of the rib cage and diaphragm during sleep | Q40099508 | ||
| Update and perspective on noninvasive respiratory muscle aids. Part 2: The expiratory aids | Q40751774 | ||
| Marked improvement of glycaemic control with pioglitazone in a Type 2 diabetic patient associated with Charcot‐Marie‐Tooth disease | Q44444561 | ||
| Charcot-Marie-Tooth Disease with Diaphragmatic Weakness | Q45399897 | ||
| Evaluation of phrenic nerve and pulmonary function in hereditary motor and sensory neuropathy, type I | Q45939342 | ||
| Electrodiagnostic Evidence of Phrenic Nerve Demyelination in Charcot-Marie-Tooth Disease 1A | Q47607054 | ||
| Changes in excitability of motor cortical circuitry in primary restless legs syndrome | Q48090141 | ||
| Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study. | Q48702662 | ||
| Daytime somnolence in myotonic dystrophy | Q48760814 | ||
| Evidence of peripheral axonal neuropathy in primary restless legs syndrome | Q48827106 | ||
| Neurodegeneration is associated to changes in serum insulin-like growth factors | Q49157579 | ||
| Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. | Q51714031 | ||
| Respiratory muscle weakness in Charcot-Marie-Tooth disease. A field study. | Q53409464 | ||
| Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2 | Q55670641 | ||
| Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis | Q56008645 | ||
| Spinal deformity associated with heritable neurological conditions: spinal muscular atrophy, Friedreich's ataxia, familial dysautonomia, and Charcot-Marie-Tooth disease | Q67748653 | ||
| Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I | Q68462463 | ||
| Phrenic involvement in Charcot-Marie-Tooth disease. A pathologic documentation | Q69358346 | ||
| Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease) | Q69784343 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | sleep | Q35831 |
| P304 | page(s) | 1-7 | |
| P577 | publication date | 2007-02-01 | |
| P1433 | published in | Lung | Q15765075 |
| P1476 | title | Disorders of Pulmonary Function, Sleep, and the Upper Airway in Charcot-Marie-Tooth Disease | |
| P478 | volume | 185 |
| Q34383346 | Advances in Positive Airway Pressure Treatment Modalities for Hypoventilation Syndromes |
| Q36976445 | Anesthetic Management of a Patient With Charcot-Marie-Tooth Disease |
| Q99248320 | CMTM6 expressed on the adaxonal Schwann cell surface restricts axonal diameters in peripheral nerves |
| Q37773629 | Canine inherited motor and sensory neuropathies: an updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease |
| Q38604756 | Charcot-Marie-Tooth 1A: A narrative review with clinical and anatomical perspectives |
| Q28111977 | Diagnosis, natural history, and management of Charcot–Marie–Tooth disease |
| Q37807192 | Diagnostic Criteria for the Classification of Vocal Cord Dysfunction |
| Q35588965 | Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis |
| Q35083966 | Fatigue, reduced sleep quality and restless legs syndrome in Charcot-Marie-Tooth disease: a web-based survey |
| Q58130386 | Fontan Failure Secondary to Charcot-Marie-Tooth-Induced Phrenic Neuropathy |
| Q57515229 | Histological and ultrastructural evidence that recurrent laryngeal neuropathy is a bilateral mononeuropathy limited to recurrent laryngeal nerves |
| Q57469076 | Juvenile-onset polyneuropathy in American Staffordshire Terriers |
| Q26768401 | Management of Charcot-Marie-Tooth disease: improving long-term care with a multidisciplinary approach |
| Q37621814 | Mechanisms of exercise limitation and pulmonary rehabilitation for patients with neuromuscular disease. |
| Q40515513 | Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking |
| Q91871274 | Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway |
| Q35138152 | Sleep pattern in Charcot-Marie-Tooth disease type 2: report of family case series |
| Q38363677 | Therapeutic options in Charcot-Marie-Tooth diseases |
Search more.