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81 in total

1. [Neurogenic muscular atrophy of proximal and symmetrical topography simulating a myopathy. Study of 2 cases].

Authors: L HURWITZ; J LAPRESLE; R GARCIN
Journal: Rev Neurol (Paris) Date: 1961-02 Impact factor: 2.607

2. Course and symptoms of progressive infantile muscular atrophy; a follow-up study of 112 cases in Denmark.

Authors: S BRANDT
Journal: Arch Neurol Psychiatry Date: 1950-02

3. Creatine phospholinase activity in spinal muscular atrophy.

Authors: L Hetnarska; J Prot; E Sawicka
Journal: J Neurol Sci Date: 1968 Mar-Apr Impact factor: 3.181

4. The neurogenic scapulo-peroneal syndrome.

Authors: K Ricker; H G Mertens; K Schimrigk
Journal: Eur Neurol Date: 1968 Impact factor: 1.710

5. Infantile and juvenile spinal muscular atrophy.

Authors: I Hausmanowa-Petrusewicz; W Askanas; B Badurska; B Emeryk; A Fidziańska; W Garbalińska; L Hetnarska; Z Kamieniecka; J Prot; I Niebrój-Dobosz; H Jedrzejowska; E Sawicka
Journal: J Neurol Sci Date: 1968 Mar-Apr Impact factor: 3.181

6. Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child.

Authors: V Dubowitz; S Roy
Journal: Brain Date: 1970 Impact factor: 13.501

7. Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree.

Authors: H Tsukagoshi; H Shoji; T Furukawa
Journal: Neurology Date: 1970-12 Impact factor: 9.910

8. Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form.

Authors: G M Fenichel; E S Emery; P Hunt
Journal: Arch Neurol Date: 1967-09

9. Benign spinal muscular atrophy arising in childhood and adolescence.

Authors: D Gardner-Medwin; P Hudgson; J N Walton
Journal: J Neurol Sci Date: 1967 Jul-Aug Impact factor: 3.181

10. Microcephaly and mental subnormalitiy in chronic progressive spinal muscular atrophy of childhood.

Authors: A J Spiro; M H Fogelson; A C Goldberg
Journal: Dev Med Child Neurol Date: 1967-10 Impact factor: 5.449

40 in total

1. Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.

Authors: H B Szliwowski; P Drochmans
Journal: Acta Neuropathol Date: 1975 Impact factor: 17.088

2. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

Authors: J Melki; S Abdelhak; P Burlet; V Raclin; J Kaplan; R Spiegel; S Gilgenkrantz; N Philip; M L Chauvet; Y Dumez
Journal: J Med Genet Date: 1992-03 Impact factor: 6.318

3. Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophy.

Authors: Erin N Wakeling; Béatrice Joussemet; Patrick Costiou; Dominique Fanuel; Philippe Moullier; Martine Barkats; John C Fyfe
Journal: J Comp Neurol Date: 2012-06-01 Impact factor: 3.215

The nosology of the spinal muscular atrophies.

1. [Neurogenic muscular atrophy of proximal and symmetrical topography simulating a myopathy. Study of 2 cases].

2. Course and symptoms of progressive infantile muscular atrophy; a follow-up study of 112 cases in Denmark.

3. Creatine phospholinase activity in spinal muscular atrophy.

4. The neurogenic scapulo-peroneal syndrome.

5. Infantile and juvenile spinal muscular atrophy.

6. Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child.

7. Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree.

8. Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form.

9. Benign spinal muscular atrophy arising in childhood and adolescence.

10. Microcephaly and mental subnormalitiy in chronic progressive spinal muscular atrophy of childhood.

1. Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.

2. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

3. Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophy.

4. Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw.

5. A family of juvenile proximal spinal muscular atrophy with dominant inheritance.

6. An investigative journalist looks at medical ethics.

7. Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?

8. Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy.

9. Segregation analysis of chronic childhood spinal muscular atrophy.

10. Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy.