Published in J Pediatr on April 01, 1969
Leprechaunism: an inherited defect in a high-affinity insulin receptor. Am J Hum Genet (1985) 1.27
Primary defect of insulin receptors in skin fibroblasts cultured from an infant with leprechaunism and insulin resistance. Proc Natl Acad Sci U S A (1979) 1.02
Leprechaunism with mosaicism 46, XX/47, XX extra ring chromosome. J Med Genet (1977) 0.99
The Patterson syndrome, leprechaunism, and pseudoleprechaunism. J Med Genet (1981) 0.89
Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease. N Engl J Med (1994) 4.46
HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society. Med Pediatr Oncol (1997) 2.59
Laparoscopic hysterectomy--is there a benefit? N Engl J Med (1996) 2.14
Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21. Am J Hum Genet (1975) 2.08
Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes. Am J Hum Genet (1973) 1.77
Genetically determined sex-reversal in 46,XY humans. Science (1978) 1.76
X-autosome translocations: a review. Birth Defects Orig Artic Ser (1978) 1.57
Enteric duplications. Thirty-seven cases: a vascular theory of pathogenesis. Am J Dis Child (1971) 1.48
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases. Clin Genet (1977) 1.45
A single blood culture for confirmation of the diagnosis of neonatal septicemia. Am J Clin Pathol (1972) 1.43
Vaginal cuff closure at abdominal hysterectomy: comparing sutures with absorbable staples. Obstet Gynecol (1991) 1.39
Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation. Am J Dis Child (1971) 1.38
The relation of Langerhans cell histiocytosis to acute leukemia, lymphomas, and other solid tumors. The LCH-Malignancy Study Group of the Histiocyte Society. Hematol Oncol Clin North Am (1998) 1.33
Cyclophosphamide in the treatment of idiopathic lipoid nephrosis. J Pediatr (1967) 1.28
Histiocytosis syndromes in children. Lancet (1987) 1.26
De-novo G-G-translocation Down's syndrome in two siblings. Lancet (1969) 1.25
Renal tumors in the neonatal period. Cancer (1968) 1.25
Neonatal small left colon syndrome. Am J Roentgenol Radium Ther Nucl Med (1974) 1.21
Professional attitudes toward the autopsy. A survey of clinicians and pathologists. Am J Clin Pathol (1989) 1.20
Nonhemolytic group B streptococcal infections. J Pediatr (1976) 1.15
Nosology and pathology of Langerhans cell histiocytosis. Hematol Oncol Clin North Am (1998) 1.14
The Interregional Cytogenetic Register System (ICRS). Birth Defects Orig Artic Ser (1978) 1.13
Langerhans' cell histiocytosis (histiocytosis X): immunophenotype and growth fraction. Hum Pathol (1993) 1.13
X-autosome translocation in normal mother and effectively 21-monosomic daughter. J Pediatr (1974) 1.09
Duplications of the alimentary tract: report of three unusual cases associated with bile and pancreatic ducts. Surgery (1972) 1.08
Cytogenetics in mentally defective children with anomalies: a controlled study. J Pediatr (1969) 1.08
Noonan's syndrome and Ebstein's malformation of the tricuspid valve. Am J Dis Child (1968) 1.05
Successful treatment of lymphohistiocytic reticulosis with phagocytosis with epipodophyllotoxin VP 16-213. Cancer (1980) 1.04
Ocular manifestations of the Rubinstein-Taybi syndrome. Case report and review of the literature. Arch Ophthalmol (1968) 1.03
Phenotypic heterogeneity in the Noonan syndrome. Birth Defects Orig Artic Ser (1979) 1.02
Histiocytosis X. Hum Pathol (1983) 1.02
Central nervous system disease in Langerhans cell histiocytosis. Hematol Oncol Clin North Am (1998) 1.01
Disseminated intravascular and cardiac thrombosis of the neonate. Am J Dis Child (1974) 1.00
Diploid-triploid mosaicism: delineation of the syndrome. Ann Genet (1983) 0.97
Acute leukemia in association with Langerhans cell histiocytosis. Med Pediatr Oncol (1994) 0.97
Accelerated skeletal maturation in infancy syndrome: report of a third case. J Pediatr (1973) 0.96
Pseudovaginal perineoscrotal hypospadias. Clin Genet (1972) 0.96
Duplication 6q syndrome. Am J Med Genet (1979) 0.95
The Russell-Silver syndrome without asymmetry. J Pediatr (1971) 0.95
Central nervous system disease in Langerhans cell histiocytosis. Br J Cancer Suppl (1994) 0.95
Tetraploidy and 18-trisomy in a six-year-old triple mosaic boy. Cytogenetics (1971) 0.95
Immature teratoma of the ovary with a neural component ("solid" teratoma). A clinicopathologic study of 20 cases. Hum Pathol (1976) 0.94
Hypohidrotic ectodermal dysplasia with multiple associated anomalies. Birth Defects Orig Artic Ser (1971) 0.93
Chromosomal aberrations with normal phenotype: four examples. Ala J Med Sci (1966) 0.93
Racial differences in the frequency of Q and C chromosomal heteromorphisms. Nature (1977) 0.92
Cervical cytology: a randomized comparison of four sampling methods. Am J Obstet Gynecol (1992) 0.92
Turner syndrome and Noonan's syndrome. J Pediatr (1969) 0.91
Adrenal abscess in a neonate. J Pediatr (1970) 0.90
Fatal airsacculitis and pneumonia, with abortion, in an orangutan. J Am Vet Med Assoc (1980) 0.90
Balanced reciprocal X-4 translocation in a female patient with early secondary amenorrhea. Am J Obstet Gynecol (1977) 0.90
Multiple congenital diverticula of the vermiform appendix. Am J Clin Pathol (1968) 0.89
Electron microscopy in histiocytosis X. Ultrastruct Pathol (1982) 0.89
Extended combination therapy of childhood rhabdomyosarcoma. Cancer (1973) 0.88
Outpatient vaginal hysterectomy as a new trend in gynecology. AORN J (1995) 0.88
Outpatient vaginal hysterectomy: a pilot study. Obstet Gynecol (1992) 0.86
Rhabdomyosarcoma in children: ultrastructural study of 31 cases. Cancer (1980) 0.86
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family. Ann Genet (1977) 0.85
Familial 2/3 translocation. Am J Hum Genet (1966) 0.85
Foamy changes of placental cells in fetal storage disorders. Virchows Arch A Pathol Anat Histol (1976) 0.85
Russell dwarf versus Silver syndrome. J Pediatr (1972) 0.84
The pathology of "histiocytosis". Am J Pediatr Hematol Oncol (1981) 0.84
Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity. N Engl J Med (1974) 0.84
Congenital androgen insensitivity due to a qualitatively abnormal androgen receptor. Am J Med Genet (1981) 0.84
Advances in the care of the child with cancer. The importance of histologic subclassification of tumors. Cancer (1986) 0.84
Congenital hepatoblastoma and Beckwith-Wiedemann syndrome: a case study including DNA ploidy profiles of tumor and adrenal cytomegaly. Pediatr Pathol (1991) 0.83
Criteria for the discontinuation of antibiotic therapy during presumptive treatment of suspected neonatal infection. Pediatr Infect Dis (1983) 0.83
Abundant expression of CD40 and CD40-ligand (CD154) in paediatric Langerhans cell histiocytosis lesions. Eur J Cancer (2000) 0.83
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family. Birth Defects Orig Artic Ser (1976) 0.82
Idiopathic adrenal hypoplasia in children. Am J Clin Pathol (1972) 0.82
GnRH agonist and iron versus placebo and iron in the anemic patient before surgery for leiomyomas: a randomized controlled trial. Leuprolide Acetate Study Group. Obstet Gynecol (1995) 0.82
Practice management in obstetrics and gynecology residency curriculum. Obstet Gynecol (1999) 0.82
Retroperitoneal lymphangioma: an unusual cause of the acute surgical abdomen. J Pediatr Surg (1973) 0.81
The Dubowitz syndrome. Am J Med Genet (1978) 0.81
Familial paroxysmal rhabdomyolysis in children. A myoglobinuric syndrome. Am J Med (1967) 0.81
S-100 protein immunohistochemistry and electron microscopy in the diagnosis of Langerhans cell proliferative disorders: a comparative assessment. Ultrastruct Pathol (1986) 0.81
Giant blood cyst and congenital pulmonic stenosis. Report of a case. Am J Dis Child (1975) 0.81
Neurologic manifestations of the Noonan syndrome. South Med J (1973) 0.80
Hyperthecosis: an inheritable form of polycystic ovarian disease. Birth Defects Orig Artic Ser (1975) 0.80
Mesoectodermal dysplasia of the iris and cornea, mental retardation and myopathy: a sporadic case. Birth Defects Orig Artic Ser (1971) 0.80
Reproduction in a woman with mosaicism. J Med Genet (1978) 0.80
Peritoneal closure at vaginal hysterectomy: a reassessment. Obstet Gynecol (1996) 0.80
Behavior of vital and killed autologous pericardium in the descending aorta of sheep. J Thorac Cardiovasc Surg (1999) 0.79
Smith-Lemli-Opitz syndrome in a negro child. J Pediatr (1969) 0.79
High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements. Hum Genet (1983) 0.79
Delineation of Robertsonian translocations in man by means of chromosome banding. Eur J Pediatr (1977) 0.79
Incidence of nickel-induced sister-chromatid exchange. Mutat Res (1982) 0.78
Diphtherial myocardiopathy. Am J Cardiol (1972) 0.78
Genetic amniocentesis: a twelve years' experience. Am J Med Genet (1985) 0.78
Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation. Eur J Pediatr (1977) 0.78
Thromboembolism and cor pulmonale complicating ventriculovenous shunt. JAMA (1967) 0.78
Incidence of major chromosome abnormalities in children. Cytogenet Cell Genet (1977) 0.78
Malignant peritoneal mesothelioma in a child. Pediatr Pathol (1986) 0.77
Polycystic ovarian disease, maturation arrest of spermiogenesis, and Klinefelter's syndrome in siblings of a family with familial hirsutism. Fertil Steril (1975) 0.77
Chromosome nomenclature. J Pediatr (1970) 0.76
Partial trisomy for different segments of chromosome 13 in several individuals of the same family. Birth Defects Orig Artic Ser (1975) 0.76
Features of Turner's syndrome in women with polycystic ovaries. Obstet Gynecol (1975) 0.76
A model for resident surgical training in laparoscopic sterilization. Obstet Gynecol (1994) 0.76
Histiocytes and histiocytosis. Blood (1995) 0.75
Autosomal syndromes. Pediatr Ann (1978) 0.75