| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0387-7604(86)80093-6 |
| P698 | PubMed publication ID | 3541664 |
| P2093 | author name string | H B Sarnat | |
| P2860 | cites work | Congenital Muscle Fiber-Type Disproportion in Krabbe's Leukodystrophy | Q70898839 |
| Emery‐dreifuss humeroperoneal muscular dystorphy: An X‐linked myopathy with unusual contractures and bradycardia | Q70965803 | ||
| Nonprogressive congenital neuromuscular disease with uniform type 1 fiber | Q71094250 | ||
| Congenital type II fibre deficient myopathy | Q71185364 | ||
| Patterns of muscle fiber-type disproportion in hypotonic infants | Q71249912 | ||
| Experimental and immunohistochemical studies on the cerebellar substance p of the rat: Localization, postnatal ontogeny and ways of entry to the cerebellum | Q72663846 | ||
| Adaptive transformation of rat soleus motor units during growth | Q39766462 | ||
| Histological Patterns of Muscle in Infants with Developmental Brain Abnormalities | Q41936537 | ||
| Cerebral influence on muscle fiber typing. The effect of fetal immobilization | Q41938986 | ||
| Human cerebellar hypoplasia: a syndrome of diverse causes | Q43468193 | ||
| Significance of impulse activity in the transformation of skeletal muscle type | Q44575408 | ||
| Central core disease or not? Observations on a family with a non-progressive myopathy | Q48633781 | ||
| A morphological study of non-Japanese congenital muscular dystrophy associated with cerebral lesions. | Q48830676 | ||
| The cerebral defect and myopathy in Duchenne muscular dystrophy A comparative clinicopathological study | Q48923804 | ||
| Ontogeny of somatostatin-containing neuron system of the rat cerebellum including its fiber connections: an experimental and immunohistochemical analysis. | Q48964040 | ||
| The central nervous system in Duchenne muscular dystrophy | Q49095766 | ||
| The mechanism of cerebellar hypotonia. An experimental study in the monkey | Q49114993 | ||
| The functional organization of the motor system in the monkey. II. The effects of lesions of the descending brain-stem pathways. | Q51190110 | ||
| The cerebral defect and myopathy in myotonic dystrophy: A comparative clinicopathological study | Q51202972 | ||
| Mental deficiency associated with muscular dystrophy. A neuropathological study. | Q51226279 | ||
| Involvement of the central nervous system in congenital muscular dystrophies. | Q52282708 | ||
| Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family | Q56232743 | ||
| Nonprogressive Congenital Neuromuscular Disease With Uniform Type 1 Fiber | Q56459981 | ||
| Delay in the maturation of muscle fibers in infants with congenital hypotonia | Q67429638 | ||
| Fukuyama-type congenital muscular dystrophy | Q70455756 | ||
| Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement | Q70568955 | ||
| A genetic study of the Fukuyama type congenital muscular dystrophy | Q70664926 | ||
| Arthrogryposis multiplex congenita in an infant with posterior agenesis of the corpus callosum | Q70664928 | ||
| Fukuyama type congenital muscular dystrophy--two Dutch siblings | Q70664936 | ||
| Congenital cervical spinal atrophy | Q70701662 | ||
| Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations | Q70859118 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 495-499 | |
| P577 | publication date | 1986-01-01 | |
| P1433 | published in | Brain and Development | Q15750896 |
| P1476 | title | Cerebral dysgeneses and their influence on fetal muscle development | |
| P478 | volume | 8 |
| Q41136840 | Clinical features of the early stage of the Rett syndrome |
| Q45869436 | Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. |
| Q69802025 | Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation |
| Q35106557 | Congenital myopathies: Natural history of a large pediatric cohort |
| Q44117669 | Do the corticospinal and corticobulbar tracts mediate functions in the human newborn? |
| Q52220844 | Expression of growth associated protein 43 and neural cell adhesion molecule in congenital fibre type disproportion with interstitial myositis. |
| Q70396994 | Lissencephaly |
| Q48914593 | Neuromuscular disorders associated with cerebral malformations |
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