Published in J Med Genet on October 01, 1977
Tibial hemimelia: new classification and reconstructive options. J Child Orthop (2016) 0.78
A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities. Am J Hum Genet (1970) 1.45
Bilateral absence of the tibias in three sibs. Birth Defects Orig Artic Ser (1974) 0.99
An unusual limb deformity in an inbred community. Birth Defects Orig Artic Ser (1974) 0.98
Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease). Clin Genet (1971) 2.51
Absence of distal interphalangeal creases of fingers with flexion limitation. J Med Genet (1976) 2.05
X-linked mental retardation and-or hydrocephalus. Clin Genet (1972) 1.81
Polysyndactyly and Marfan's syndrome. J Med Genet (1974) 1.54
Prevalence of glycosuria and diabetes among Indians and Bantu. S Afr Med J (1969) 1.50
Differential role of GDNF and NGF in the maintenance of two TTX-resistant sodium channels in adult DRG neurons. Brain Res Mol Brain Res (1999) 1.40
Chorea associated with systemic lupus erythematosus in children. A case report. Isr J Med Sci (1989) 1.40
Appendiceal obstruction by a toothpick removed at colonoscopy. Am J Gastroenterol (1986) 1.33
Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance. J Med Genet (1971) 1.32
Plasticity of sodium channel expression in DRG neurons in the chronic constriction injury model of neuropathic pain. Pain (1999) 1.27
Cystic lymphangioma of the pancreas: CT and pathologic findings. Abdom Imaging (1998) 1.22
Expression of the intermediate filament nestin during rodent tooth development. Int J Dev Biol (1995) 1.22
Inheritance of idiopathic torsion dystonia among Jews. J Med Genet (1984) 1.20
Characterization of glial trkB receptors: differential response to injury in the central and peripheral nervous systems. Proc Natl Acad Sci U S A (1993) 1.19
Prenatal diagnosis and the pediatric surgeon: the impact of prenatal consultation on perinatal management. J Pediatr Surg (1996) 1.11
Peritoneal encapsulation in childhood. Case report, embryologic analysis, and review of literature. Am J Surg (1979) 1.11
GDNF mRNA in Schwann cells and DRG satellite cells after chronic sciatic nerve injury. Neuroreport (1996) 1.09
Increased levels of trkB mRNA and trkB protein-like immunoreactivity in the injured rat and cat spinal cord. Proc Natl Acad Sci U S A (1992) 1.08
Shingles during the course of treatment with 6-mercaptopurine for inflammatory bowel disease. Am J Gastroenterol (1999) 1.07
Structural basis of sympathetic-sensory coupling in rat and human dorsal root ganglia following peripheral nerve injury. J Neurocytol (1999) 1.06
A familial syndrome of central nervous system and ocular malformations. Clin Genet (1975) 1.06
Chronic Gaucher's disease; clinical observations on 34 patients. Isr J Med Sci (1965) 1.05
Triplet and quadruplet pregnancies and management. Obstet Gynecol (1981) 1.05
Phase I and pharmacokinetic study of two sequences of gemcitabine and docetaxel administered weekly to patients with advanced cancer. Cancer Chemother Pharmacol (2001) 1.04
Regrowth of motor axons following spinal cord lesions: distribution of laminin and collagen in the CNS scar tissue. Brain Res Bull (1993) 1.03
Thin ribs in neonatal myotonic dystrophy. Clin Genet (1975) 1.03
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. Am J Hum Genet (1977) 1.03
Some effects on the offspring of uncle-niece marriage in the Moroccan Jewish community in Jerusalem. Am J Hum Genet (1974) 1.02
Anti-M, a new antibody of the MNS blood group system. I. Mv, a new inherited variant of the M gene. Am J Hum Genet (1966) 1.02
Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family. J Med Genet (1972) 1.00
Teeth and tooth nerves. Prog Neurobiol (1995) 1.00
Autosomal recessive hydrotic ectodermal dysplasia. J Med Genet (1977) 0.99
Spinal axons in central nervous system scar tissue are closely related to laminin-immunoreactive astrocytes. Neuroscience (1995) 0.98
Mental retardation and congenital malformations associated with a ring chromosome 6. Clin Genet (1975) 0.97
Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Clin Genet (1972) 0.96
A score based on eight signs in the diagnosis of Down syndrome in the newborn. J Ment Defic Res (1980) 0.96
Reactivation of Delta-Notch signaling after injury: complementary expression patterns of ligand and receptor in dental pulp. Exp Cell Res (1999) 0.96
Sodium channel expression in NGF-overexpressing transgenic mice. J Neurosci Res (1999) 0.95
A lethal autosomal recessive entero-colitis of early infancy. Clin Genet (1974) 0.95
Adventitial cystic disease. J Foot Surg (1991) 0.95
Giant pseudopolyposis in colitis with colonic intussusception. Gastroenterology (1978) 0.94
[Course and pathogenesis of neurotrophic osteoarthropathies]. Fortschr Geb Rontgenstr Nuklearmed (1970) 0.94
Recurrent pancreatitis caused by vegetable matter obstruction. Am J Gastroenterol (1986) 0.94
[Faulty origin of the right subclavian artery from the pulmonary artery: a rare cause of subclavian steal syndrome in childhood]. Monatsschr Kinderheilkd (1991) 0.93
Relatively high prevalence of the Meckel syndrome among Jews. Isr J Med Sci (1974) 0.92
Differential expression of sodium channel genes in retinal ganglion cells. Brain Res Mol Brain Res (1997) 0.92
Purine base incorporation into erythrocyte nucleotides in hypoxanthine-guanine phosphoribosyltransferase deficiency. Biochem Med (1971) 0.91
Cellular expression of neurotrophin mRNAs during tooth development. Cell Tissue Res (1997) 0.91
Probable autosomal recessive Marfan syndrome. J Med Genet (1977) 0.91
Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis). Clin Genet (1981) 0.91
In vivo NGF deprivation reduces SNS expression and TTX-R sodium currents in IB4-negative DRG neurons. J Neurophysiol (1999) 0.90
Effectiveness, reproducibility, and weight-relation of screening-tests for diabetes. Lancet (1968) 0.90
Echinococcosis presenting as a supraclavicular mass. Successful therapy with mebendazole. Clin Pediatr (Phila) (1982) 0.90
Prevention of the respiratory distress syndrome in premature infants by antepartum glucocorticoid therapy. Br J Obstet Gynaecol (1976) 0.90
High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel. Clin Genet (1977) 0.89
Neurotoxicity after spinal anaesthesia induced by serial intrathecal injections of magnesium sulphate. An experimental study in a rat model. Anaesthesia (1997) 0.89
Tubular ectasia of the rete testis: an ultrasound diagnosis. Urology (1995) 0.89
Myelin sheath thickness and internodal length of nerve fibres in the developing feline inferior alveolar nerve. J Neurol Sci (1982) 0.89
Familial thyroglossal duct cyst. Clin Genet (1993) 0.87
Probable autosomal dominant infantile pyloric stenosis in a large kindred. Clin Genet (1981) 0.87
The old beliefs and the cerebral palsied. Rehabil Rec (1968) 0.87
Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus. J Med Genet (1973) 0.87
Changes in nerve growth factor receptor-like immunoreactivity in the spinal cord after ventral funiculus lesion in adult cats. J Neurocytol (1992) 0.87
In vitro - in vivo correlation of gene expression alterations induced by liver carcinogens. Curr Med Chem (2012) 0.87
Familial primary vesicoureteral reflux. Clin Genet (1975) 0.87
Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. J Med Genet (1969) 0.87
[Aseptic necroses of the patella]. Cesk Radiol (1970) 0.87
The outcome of pregnancy after gonadotrophin therapy. Br J Obstet Gynaecol (1976) 0.87
Sugar intake and diabetes. Diabetes (1967) 0.86
Distribution and axonal relations of macrophages in a neuroma. Neuroscience (1993) 0.86
Sympathetic nerve sprouting fails to occur in the trigeminal ganglion after peripheral nerve injury in the rat. Pain (1999) 0.86
Multiple meningiomas in separate neuroaxial compartments in a child. Childs Brain (1980) 0.86
Congenital afibrinogenemia in 10 offspring of uncle-niece marriages. Clin Genet (1980) 0.85
Distribution of P2X3 receptors in the rat trigeminal ganglion after inferior alveolar nerve injury. Neurosci Lett (1998) 0.85
Angiodysplasia of the colon. J R Soc Med (1987) 0.85
Legionnaires' Disease in Israel: serological evidence of childhood infection. Isr J Med Sci (1983) 0.85
Inferior alveolar nerve regeneration and incisor pulpal reinnervation following intramandibular neurotomy in the cat. Brain Res (1982) 0.85
Growth of ascending spinal axons in CNS scar tissue. Int J Dev Neurosci (1993) 0.85
Primary retroperitoneal soft-tissue sarcomas. J Surg Oncol (1984) 0.85
Pulmonary veno-occlusive disease in a unilateral hypertransradiant lung. Thorax (1981) 0.85
AIDS-related lymphoma: an unusual cause of omental caking. AJR Am J Roentgenol (1993) 0.84
Ring chromosome 13 syndrome. Clin Genet (1975) 0.84
Neuropeptide- and tyrosine hydroxylase-immunoreactive nerve fibers in painful Morton's neuromas. Muscle Nerve (2000) 0.84
Autosomal recessive lethal infantile cytochrome C oxidase deficiency. Am J Dis Child (1991) 0.84
Substance P-, calcitonin gene-related peptide, growth-associated protein-43, and neurotrophin receptor-like immunoreactivity associated with unmyelinated axons in feline ventral roots and pia mater. J Comp Neurol (1994) 0.83
Congenital contractural arachnodactyly in two double second cousins: possible homozygosity. Clin Genet (1993) 0.83
Pulpal axons in developing, mature, and aging feline permanent incisors. A study by electron microscopy. J Comp Neurol (1981) 0.83
Infantile neuroaxonal dystrophy. Confin Neurol (1970) 0.83
Solitary eosinophilic granuloma of sternum: case report with review of the literature. Br J Radiol (1985) 0.83
[Osteo-onycho dysplasia]. Z Orthop Ihre Grenzgeb (1965) 0.83
Expression of HMGB1 during tooth development. Cell Tissue Res (2006) 0.83
Abnormal expression of SNS/PN3 sodium channel in cerebellar Purkinje cells following loss of myelin in the taiep rat. Neuroreport (1999) 0.82
NGF, BDNF, NT3, NT4 and GDNF in tooth development. Eur J Oral Sci (1998) 0.82