Published in Am J Dis Child on November 01, 1964
The pathology of Tangier disease. A light and electron microscopic study. Am J Pathol (1975) 1.26
Inborn errors of metabolism in neurology (Wilson's disease, Refsum's disease and lipidoses). Proc R Soc Med (1971) 1.20
Lipid abnormalities in a variant of the Hurler syndrome. Proc Natl Acad Sci U S A (1968) 1.00
Studies on GM1-gangliosidosis, type II. Acta Neuropathol (1974) 0.98
The liver in lipidosis. An electron miscroscopic and histochemical study. Am J Pathol (1966) 0.96
Pathology of Tangier disease. J Clin Pathol (1971) 0.93
Ganglioside biochemistry. ISRN Biochem (2012) 0.89
I-cell disease. A further report on its pathology. Acta Neuropathol (1984) 0.86
Mucopolysaccharidoses and mucolipidoses. J Clin Pathol Suppl (R Coll Pathol) (1974) 0.84
Gm1 gangliosidosis associated with neonatal-onset of diffuse ecchymoses and mongolian spots. Indian J Dermatol (2011) 0.81
Alterations of astrocytic organelles in various lipidoses and allied diseases. Acta Neuropathol (1971) 0.81
Canine GM1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different models. Am J Pathol (1992) 0.80
GM1 gangliosidosis type 1 in twins. J Med Genet (1977) 0.80
GM1 gangliosidosis (type 1) in a cat. Biochem J (1986) 0.79
GM1-generalized gangliosidosis variant with cardiomegaly. Postgrad Med J (1976) 0.79
Corneal clouding in GM1-generalized gangliosidosis. Br J Ophthalmol (1976) 0.78
Hepatic storage of oligosaccharides and glycolipids in a cat affected with GM1 gangliosidosis. Biochem J (1978) 0.77
Analysis of urinary oligosaccharides in lysosomal storage disorders by capillary high-performance anion-exchange chromatography-mass spectrometry. Anal Bioanal Chem (2012) 0.76
Chemical studies in gargoylism. Arch Dis Child (1967) 0.75
Sphingolipidoses. Calif Med (1971) 0.75
Electrocardiographic and biochemical abnormalities in Tay-Sachs disease. Bull N Y Acad Med (1971) 0.75
Early characteristic radiographic changes in mucolipidosis II. Pediatr Radiol (2016) 0.75
The battered-child syndrome. JAMA (1962) 18.61
The localization of homolgous plasma proteins in the tissues of young human beings as demonstrated with fluorescent antibodies. J Exp Med (1953) 5.79
Clinical investigations on attenuated strains of poliomyelitis virus; use as a method of immunization of children with living virus. J Am Med Assoc (1956) 4.31
A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics (1954) 3.69
Purulent meningitis of newborn infants. Eleven-year experience in the antibiotic era. N Engl J Med (1961) 3.28
The nature of the hyaline membrane in asphyxia of the newborn. Pediatrics (1956) 3.25
Studies on copper metabolism I. A method for the determination of copper in whole blood, red blood cells, and plasma. J Biol Chem (1952) 3.12
Total pulmonary venous drainage into the right side of the heart; report of 17 autopsied cases not associated with other major cardiovascular anomalies. Lab Invest (1957) 3.04
Studies on the nature of fibrinoid in the collagen diseases. Am J Pathol (1957) 2.77
The roentgen manifestations of unrecognized skeletal trauma in infants. Am J Roentgenol Radium Ther Nucl Med (1953) 2.62
A syndrome of recurrent infection and infiltration of viscera by pigmented lipid histiocytes. Pediatrics (1957) 2.44
Experimental nephrotic syndrome induced in rats by aminonucleoside; renal lesions and body electrolyte composition. Proc Soc Exp Biol Med (1955) 2.43
Studies on copper metabolism. IX. The transportation of copper in blood. J Clin Invest (1953) 2.16
THIRTEEN BOYS WITH PROGRESSIVE SEPTIC GRANULOMATOSIS. Pediatrics (1965) 2.10
Isolation of intranuclear inclusion producing agents from infants with illnesses resembling cytomegalic inclusion disease. Proc Soc Exp Biol Med (1957) 2.05
Persistence of measles virus and depression of antibody formation in patients with giant-cell pneumonia after measles. N Engl J Med (1959) 1.92
Histoplasmosis. Am J Med (1955) 1.89
Amnion nodosum: a lesion of the placenta apparently associated with deficient secretion of fetal urine. Am J Obstet Gynecol (1950) 1.87
Maternal autoimmunization to thyroid as a probable cause of athyrotic cretinism. N Engl J Med (1960) 1.87
Form of hepatitis in neonatal period simulating biliary atresia. AMA Arch Pathol (1952) 1.86
Studies on copper metabolism. II. Hematologic manifestations of copper deficiency in swine. Blood (1952) 1.80
Variations in the staining characteristics of human fibrin. Am J Pathol (1957) 1.80
Studies on copper metabolism. VII. Blood copper in pregnancy and various pathologic states. J Clin Invest (1953) 1.79
Pulmonary mechanics during induced pulmonary edema in anesthetized dogs. J Appl Physiol (1959) 1.76
THE EFFECT OF IMMATURITY AND PRENATAL ASPHYXIA ON THE LUNGS AND PULMONARY FUNCTION OF NEWBORN LAMBS: THE EXPERIMENTAL PRODUCTION OF RESPIRATORY DISTRESS. Pediatrics (1965) 1.73
A fat absorption test using iodized oil, with particular application as a screening test in the diagnosis of fibrocystic disease of the pancreas. Pediatrics (1955) 1.71
Significance of selective vasculitis and the "bone-marrow" syndrome in Pseudomonas septicemia. N Engl J Med (1961) 1.64
Calcification of the intervertebral disks in childhood. Radiology (1954) 1.62
TREATMENT OF RETICULOENDOTHELIOSIS WITH VINBLASTINE SULFATE: PRELIMINARY REPORT. J Pediatr (1963) 1.61
The site of synthesis of the 19S gamma-globulins in dysgammaglobulinemia. J Exp Med (1962) 1.58
Familial Addison's disease; case reports of two sisters with corticoid deficiency unassociated with hypoaldosteronism. AMA J Dis Child (1959) 1.56
THE THYMUS AND OTHER LYMPHOID TISSUES IN CONGENITAL AGAMMAGLOBULINEMIA. I. THYMIC ALYMPHOPLASIA AND LYMPHOCYTIC HYPOPLASIA AND THEIR RELATION TO INFECTION. Pediatrics (1963) 1.53
Deciduous teeth as an index of body burden of lead. J Pediatr (1962) 1.52
The syndrome of familial juvenile hypoadrenocorticism, hypoparathyroidism and superficial moniliasis. J Clin Endocrinol Metab (1956) 1.52
Orbital hypotelorism, arhinencephaly, and trigonocephaly. Radiology (1960) 1.51
Studies on copper metabolism. III. The metabolism of iron in copper deficient swine. Blood (1952) 1.49
Studies on copper metabolism. VI. Blood copper in normal human subjects. J Clin Invest (1953) 1.47
Pulmonary hyaline membranes in newborn infants; statistical, morpho logic and experimental study of their nature, occurrence and significance. Pediatrics (1951) 1.45
Collagen disease in patients with congenital agammaglobulinemia. Trans Assoc Am Physicians (1956) 1.45
Premature obliteration of the sternal sutures and pigeon-breast deformity. Radiology (1958) 1.44
The relation of splenic calcification to histoplasmosis. N Engl J Med (1955) 1.41
Prolonged obstructive jaundice in infancy. IV. Neonatal hepatitis. AMA Am J Dis Child (1954) 1.38
An unusual osseous sequel to infantile scurvy. J Bone Joint Surg Am (1953) 1.38
Assessment of potential malignancy of cultured cells: further observations on the differentiation of "normal" and "neoplastic" cells maintained in vitro by hetero-transplantation in Syrian hamsters. Natl Cancer Inst Monogr (1962) 1.37
Iron deficiency anemia. Pediatr Clin North Am (1957) 1.34
The nature of the hyaline thrombi in thrombotic thrombocytopenic purpura. Am J Pathol (1957) 1.34
Antithyroid antibody and chronic thyroiditis in diabetes. J Clin Endocrinol Metab (1963) 1.32
Fatal infection in an infant associated with Coxsackie virus group A, type 16. N Engl J Med (1963) 1.29
THYMIC ALYMPHOPLASIA AND CONGENITAL ALEUKOCYTOSIS. Pediatrics (1964) 1.29
Immunochemical demonstration of fibrin in the generalized Shwartzman reaction. AMA Arch Pathol (1959) 1.29
ACQUIRED AGAMMAGLOBULINAEMIA IN SIBLINGS. Lancet (1965) 1.27
Chronic moniliasis associated with Addison's disease. AMA Am J Dis Child (1955) 1.26
Histochemical studies in Hurler's disease: a new method for localization of acid mucopolysaccharide, and an analysis of lead acetate "fixation". J Histochem Cytochem (1961) 1.25
Neoplasia following therapeutic irradiation for benign conditions in childhood. Radiology (1960) 1.24
FECAL RETENTION IN CHILDREN WITH CYSTIC FIBROSIS. REPORT OF THREE CASES. Pediatrics (1964) 1.24
Reparative phenomena in lungs of neonates with hyaline membranes. Pediatrics (1962) 1.23
Cirrhosis of the liver in infants and children. AMA Am J Dis Child (1955) 1.23
IMMUNOLOGIC STUDIES OF HEART TISSUE. VI. CARDIAC LESIONS IN RABBITS ASSOCIATED WITH AUTOANTIBODIES TO HEART INDUCED BY IMMUNIZATION WITH HETEROLOGOUS HEART. J Immunol (1963) 1.23
Mechanisms of brain damage in H. influenzae meningitis. J Neuropathol Exp Neurol (1960) 1.22
Congenital absence of the abdominal muscles associated with malformation of the genitourinary and alimentary tracts; report of cases and review of literature. Am J Dis Child (1950) 1.21
Histochemical properties of renal lead-inclusions and their demonstration in urinary sediment. Am J Clin Pathol (1959) 1.19
Phosphatase studies in Gaucher's disease. Metabolism (1960) 1.19
Congenital cystic adenomatoid malformation of the lung in infants. Am J Roentgenol Radium Ther Nucl Med (1956) 1.18
GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM? Am J Dis Child (1965) 1.14
Lycopenemia: a variant of carotenemia. N Engl J Med (1960) 1.13
The histology of antigenically stimulated lymph nodes in rabbits given ACTH or cortisone. Am J Pathol (1952) 1.12
Rhythmic palatal myoclonus, with a report of four cases. J Laryngol Otol (1953) 1.11
Septicemic adrenal hemorrhage. Am J Dis Child (1963) 1.11
Factors in the genesis of bile stasis in infancy. Pediatrics (1961) 1.10
Studies on copper metabolism. VIII. The correlation between the serum copper level and various serum protein fractions. J Lab Clin Med (1953) 1.09
The effects of a nitrogen mustard [tris (2-choloroethyl) amine] on regenerating rat liver. Cancer (1949) 1.08
The pathological changes in the liver in cystic fibrosis of the pancreas. AMA J Dis Child (1957) 1.06
Observations on the kidney after phosphate loading in the rat. Arch Pathol (1959) 1.05
Histochemical studies on the cerebral lipidoses and other cellular metabolic disorders. Am J Pathol (1957) 1.04
Obstructive factors in the pulmonary hyaline membrane syndrome in asphyxia of the newborn. Pediatrics (1958) 1.03
Interstitial cell tumor of the testis; study of a 5-year-old boy with pseudo-precocious puberty. J Clin Endocrinol Metab (1952) 1.02
Aldehyde-fuchsin-positive material of the posterior pituitary; its nature and significance. Lab Invest (1956) 1.01
MILK-INDUCED GASTROINTESTINAL BLEEDING IN INFANTS WITH HYPOCHROMIC MICROCYTIC ANEMIA. JAMA (1964) 1.00
Clinical pathologic conference. Neurology (1955) 1.00
Copper and protein depletion complicating hypoferric anemia of infancy. Pediatrics (1959) 1.00
Studies on copper metabolism. X. Factors influencing the plasma copper level of the albino rat. Am J Physiol (1952) 0.99
Seitelberger's spastic amaurotic axonal idiocy. Report of a case in a 9-year-old boy with comment on visceral manifestations. Pediatrics (1960) 0.97
Phosphorylation as a histochemical procedure. J Histochem Cytochem (1956) 0.97
EFFECT OF PROGESTINS, ESTROGENS AND CASTRATION ON INDUCED ENDOMETRIAL CARCINOMA IN THE RABBIT. Surg Forum (1963) 0.97
Detection of antithyroid antibodies. J Clin Endocrinol Metab (1958) 0.97
A NEW TEST FOR FAT ABSORPTION WHICH EMPLOYS AN IODINATED TRIGLYCERIDE. J Pediatr (1964) 0.97
Congenital defect of the bony orbit and pulsating exophthalmos. AMA J Dis Child (1956) 0.96
Anaplastic cells of fetal adrenal cortex. Am J Clin Pathol (1951) 0.96
Observations on disturbances of equilibrium and other symptoms induced by jet-engine noise. J Laryngol Otol (1951) 0.96
Normal blood values in infancy and childhood. Pediatr Clin North Am (1957) 0.96
Observations on magnesium deficiency in the rat. Lab Invest (1962) 0.95
Roentgen standards fo-size of the pituitary fossa from infancy through adolescence. Am J Roentgenol Radium Ther Nucl Med (1957) 0.95
The celiac syndrome. Pediatr Clin North Am (1962) 0.95
The isolation of mumps at autopsy. Am J Pathol (1949) 0.94
DISTENSIBILITY CURVES AND EXPANSION PATTERNS OF NEWBORN LUNGS. THE UNIQUE PATTERN OF LUNGS OF INFANTS WITH HYALINE MEMBRANES. Am J Dis Child (1963) 0.93
Hepatic cirrhosis and hereditary disorders of metabolism. Am J Clin Pathol (1956) 0.93