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1975, ISBN 9780803616400, x, 121
Book
Neuromuscular Disorders, ISSN 0960-8966, 02/2018, Volume 28, Issue 2, pp. 103 - 115
Spinal muscular atrophy (SMA) is a severe neuromuscular disorder due to a defect in the survival motor neuron 1 ( ) gene. Its incidence is approximately 1 in... 
Diagnosis | Nutrition | Orthopedic | Care | Phisotherapy | Spinal muscular atrophy | PHENOTYPIC VARIABILITY | EARLY-ONSET SCOLIOSIS | NEUROSCIENCES | CLINICAL NEUROLOGY | NEUROMUSCULAR SCOLIOSIS | MOTOR-NEURON GENE | GLUCOSE-METABOLISM | CLINICAL-TRIALS | OPERATIVE TREATMENT | CONTROLLED GROWING RODS | CONSENSUS STATEMENT | SMN2 COPY NUMBER | Care and treatment
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2016, Volume 99, Issue 5, pp. 1206 - 1216
Journal Article
2002, 2nd ed., ISBN 9781583331217, xii, 194
Book
Journal Article
American Family Physician, ISSN 0002-838X, 2014, Volume 89, Issue 3, pp. 193 - 198
Adolescent idiopathic scoliosis is the most common form of scoliosis, affecting approximately 2% to 4% of adolescents. The incidence of scoliosis is about the... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | CURVE PROGRESSION | PRIMARY HEALTH CARE | HEALTH | Scoliosis - therapy | Scoliosis - physiopathology | Humans | Adolescent | Mass Screening - organization & administration | Female | Male | Disease Progression | Practice Guidelines as Topic | Scoliosis - diagnosis | Scoliosis
Journal Article
Child's Nervous System, ISSN 0256-7040, 10/2019, Volume 35, Issue 10, pp. 1673 - 1679
Journal Article
Journal of the American Academy of Orthopaedic Surgeons, ISSN 1067-151X, 05/2019, Volume 27, Issue 10, pp. e462 - e472
Scheuermannʼs kyphosis (SK) is a rigid structural deformity of the thoracic spine defined radiographically as three or more contiguous vertebrae with at least... 
COMBINED ANTERIOR | SURGERY | SPINAL-FUSION | PEDICLE SCREW | DISEASE | FOLLOW-UP | COMPLICATIONS | PROXIMAL JUNCTIONAL KYPHOSIS | POSTERIOR INSTRUMENTATION | ADOLESCENT IDIOPATHIC SCOLIOSIS | ORTHOPEDICS | SURGICAL-TREATMENT
Journal Article
Spine, ISSN 0362-2436, 06/2013, Volume 38, Issue 13, pp. 1128 - 1136
Journal Article
Orthopaedics & Traumatology: Surgery & Research, ISSN 1877-0568, 02/2018, Volume 104, Issue 1, pp. S89 - S95
Neuromuscular diseases (NMDs) affect the peripheral nervous system, which includes the motor neurons and sensory neurons; the muscle itself; or the... 
Neuromuscular diseases | Neuromuscular scoliosis | Muscular dystrophy | Spinal muscular atrophy | SURGERY | ATROPHY | DUCHENNE MUSCULAR-DYSTROPHY | SPINE SURGERY | ORTHOPEDICS | SCOLIOSIS
Journal Article
01/2017, 1st ed. 2017, ISBN 9783319477077, 293
Providing a sound definition and review of the pertinent treatment goals for the management of adult lumbar scoliosis, this practical and comprehensive guide... 
Surgery | Orthopedics | Medicine & Public Health
eBook
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 04/2017, Volume 12, Issue 1, pp. 69 - 11
Background: Ring chromosome 14 syndrome is a rare chromosomal disorder characterized by early onset refractory epilepsy, intellectual disability, autism... 
Abnormality of retinal pigmentation | Autoimmunity | Caregivers | Anorexia | Respiratory insufficiency | Behavioral abnormality | Muscular hypotonia | Thin vermilion border | Dehydration | Microcephaly | Best practices | Cafe-au-lait spot | Abnormality of the retina | Osteoporosis | Intellectual disability | Respiratory failure | Ring14 syndrome | Scoliosis | Dysphagia | Constipation | Hypertelorism | Focal seizures with impairment of consciousness or awareness | Osteopenia | Downslanted palpebral fissures | Strabismus | Aspiration | Milia | Blepharophimosis | Growth delay | Celiac disease | Abnormality of the corpus callosum | Abnormality of the immune system | Autistic behavior | Stereotypy | Astigmatism | Increased body weight | Microphthalmia | Recurrent upper respiratory tract infections | Glaucoma | Pneumonia | Absent speech | Global developmental delay | Optic neuropathy | Hyperactivity | Myopia | Short stature | Abnormality of vision | Arthritis | Abnormality of the eye | Epicanthus | Recommendations | Underdeveloped supraorbital ridges | Feeding difficulties | Pain | Encephalopathy | Recurrent infections | Respiratory tract infection | Malnutrition | Status epilepticus | Seizures | Cataract | Aggressive behavior | Myoclonus | Flexion contracture | Ventriculomegaly | Brain atrophy | Coloboma | Full cheeks | Hearing impairment | Fever | Abnormality of skin pigmentation | Abnormality of the face | Autism | Diaphragmatic weakness | Facial asymmetry | Recurrent pneumonia | Horizontal eyebrow | Retinal degeneration | Focal seizures | Large forehead | Pallor | MEDICINE, RESEARCH & EXPERIMENTAL | COMPLEX PARTIAL SEIZURES | INSTABILITY | 14-CHROMOSOME | CHROMOSOME 14 SYNDROME | DEVELOPMENTAL DELAY | MECHANISMS | TERMINAL DELETIONS | PARTIAL EPILEPSY | GENETICS & HEREDITY | PATIENT | MOSAICISM | Autism Spectrum Disorder - genetics | Humans | Cytogenetics | Ring Chromosomes | Chromosome Disorders - genetics | Chromosomes, Human, Pair 14 - genetics | Intellectual disabilities | Epilepsy | Chromosome deletion | Single-nucleotide polymorphism | Gene expression | Medical diagnosis | Patients | Feeding | Genotype & phenotype | Clonal deletion | Epigenetics | Children | Chromosome 14 | Autonomy | Books | Chromosomes
Journal Article