Published in Arch Fr Pediatr on January 01, 1951
Genetic and non-genetic factors in the etiology of congenital heart disease: a study of 1188 cases. Am J Hum Genet (1957) 3.49
[PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18]. Pathol Biol (Paris) (1964) 3.32
[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT]. Arch Fr Pediatr (1964) 2.48
[Pyknodysostosis]. Presse Med (1962) 2.26
ANENECEPHALY IN FRANCE. Am J Hum Genet (1964) 1.81
THE MALADY OF TOULOUSE-LAUTREC. JAMA (1965) 1.78
[2 cases of a condensing osseous disease: pynodysostosis]. Arch Fr Pediatr (1962) 1.73
[Pseudo-achondroplastic forms of spondylo-epiphyseal dysplasias]. Presse Med (1959) 1.45
Differentiation of hemophilia into two groups; a study of thirty-three cases. N Engl J Med (1953) 1.42
[Diastrophic nanism]. Presse Med (1960) 1.41
Streptomycin and tuberculous meningitis in children; preliminary note. Br Med J (1947) 1.41
[Indications for treatment of initial tuberculosis in children and adolescents]. Presse Med (1954) 1.40
[Preparation of a fraction rich in prothrombin, proconvertin, Stuart factor and antihemophilic factor B (P.P.B. fraction)]. Pathol Biol (Paris) (1959) 1.39
[Therapeutic results in the use of human serum gamma globulins; survey of 6, 602 cases. I. Main indications for their use in infections diseases]. Presse Med (1958) 1.39
[Deficiency of antihemophilic factor A in a girl associated with bleeding disorder]. Rev Hematol (1953) 1.34
[Not Available]. Presse Med (1957) 1.30
[A NEW DYSOSTOSIS WITH URINARY ELIMINATION OF CHONDROITIN SULFATE B]. Presse Med (1963) 1.27
[Not Available]. Rev Hematol (1949) 1.25
[Biopsy of the intestinal mucosa in children. Initial results of a study of the malabsorption syndromes]. Presse Med (1963) 1.25
[Cat scratch disease]. Sem Hop (1950) 1.25
[Differential characteristics of Hageman & P.T.A. factors; role of contact in the initial phase of coagulation]. Rev Fr Etud Clin Biol (1958) 1.21
[Umbilical cord blood; complete study of its coaguability, comparison with maternal blood]. Etudes Neonatales (1952) 1.20
[Number of dermatoglyphics in twins]. Ann Hum Genet (1957) 1.20
Symptomatology and diagnosis of poliomyelitis. Monogr Ser World Health Organ (1955) 1.18
[Culture of trypsinated cells of rabbit kidney and their applications to the study of viruses of herpetic group]. Ann Inst Pasteur (Paris) (1955) 1.18
[Fatal hemorrhagic syndromes with total incoagulability and with fibrinolysis; in pulmonary exeresis]. Rev Hematol (1952) 1.15
[Analytical study on Quick test; determination of prothrombin, proconvertin, and proaccelerin]. Sang (1952) 1.15
Preparation of a human plasma fraction rich in prothrombin, proconvertin, Stuart factor, and PTC and a study of its activity and toxicity in rabbits and man. J Lab Clin Med (1959) 1.14
[Not Available]. Sem Hop (1948) 1.14
Hageman trait and PTA deficiency; the role of contact of blood with glass. Br J Haematol (1959) 1.13
Measurement of thromboplastic factors and profactors in plasma. I. Deficits in thromboplastin; study of reagents; measurements of antihemophilic and of platelet activities. J Lab Clin Med (1953) 1.13
[PROBABLE PERICENTRIC INVERSION OF THE NO. 2 CHROMOSOME AND CONGENITAL MALFORMATIONS IN A BOY]. Ann Genet (1963) 1.13
[Treatment of hemophilia B with a plasma fraction rich in antihemophilic B factor (P.P.B.)]. Pathol Biol (Paris) (1959) 1.11
Congenital absence of beta-lipoproteins. Pediatrics (1963) 1.11
[Recurrent infectious parotitis in children]. Arch Fr Pediatr (1951) 1.11
[Not Available]. Ann Hum Genet (1957) 1.09
[Diarrhea caused by disorders of the intestinal hydrolysis of saccharose, maltose and isomaltose]. Arch Fr Pediatr (1963) 1.07
[Miliary tuberculosis in children]. Lancet (1952) 1.07
[Results of an investigation of the heredity of diabetes mellitus]. Rev Fr Etud Clin Biol (1957) 1.06
[Grave hemorrhages during thoracic surgery from blood incoagulability due to fibrinolysis]. Mem Acad Chir (Paris) (1951) 1.03
TRUE HERMAPHRODITISM WITH XX-XY MOSAICISM, PROBABLY DUE TO DOUBLE FERTILIZATION OF THE OVUM. J Clin Endocrinol Metab (1965) 1.02
A new adsorption agent for coagulation factors. J Clin Pathol (1959) 1.01
[Heredity of diabetes mellitus]. Journ Annu Diabetol Hotel Dieu (1961) 1.00
Streptomycin treatment of septicaemia and meningitis due to intestinal organisms in infants. Br Med J (1949) 0.98
[17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL]. Ann Genet (1964) 0.98
[FAMILIAL ANECEPHALY AND REARRANGEMENT OF 2 13-15 CHROMOSOMES]. C R Hebd Seances Acad Sci (1964) 0.98
[Dominant acro-osteolysis]. Arch Fr Pediatr (1961) 0.96
[Electron microscope study of lymphoid leukemia with intracytoplasmic crystals]. Rev Hematol (1960) 0.96
[Bourneville's sclerosis tuberosa in infant and small child]. Arch Fr Pediatr (1952) 0.96
[USE OF HOMOTYPIC ORAL ANTIPOLIOMYELITS VACCINATION IN AN EPIDEMIC CAUSED BY TYPE I POLIOMYELITIS VIRUS IN FRANCE]. Bull World Health Organ (1964) 0.95
[Acute familial leukosis; parallel course of acute leukosis of the same type in child and father]. Bull Mem Soc Med Hop Paris (1951) 0.95
[Determinations of properdin; technical study]. Rev Fr Etud Clin Biol (1957) 0.95
[The congenital absence of beta-lipoproteins]. Presse Med (1961) 0.94
[The congenital abscence of beta-lipoproteins]. C R Seances Soc Biol Fil (1960) 0.93
[Three cases of Ollier's disease in one family]. Bull Mem Soc Med Hop Paris (1954) 0.93
[Technical modifications of the in vitro heparin tolerance test]. Sem Hop (1951) 0.93
[Dyschondroplasia. Multiple chondromatosis of the skeleton]. Sem Hop (1960) 0.92
Genetics of haemochromatosis. Ann Hum Genet (1958) 0.92
The genetics of pyloric stenosis. Proc R Soc Med (1953) 0.92
[Not Available]. Sem Hop (1949) 0.91
[Acanthocytosis. Its relations to the congenital absence of beta-lipoproteins]. Presse Med (1961) 0.91
[Metabolism of iron in the descendants of patients with bronze cirrhosis]. Bull Mem Soc Med Hop Paris (1952) 0.91
[Deletion of the short arms of chromosome 17-18: complex deformities with oligophrenia]. Arch Fr Pediatr (1963) 0.91
Systemic treatment of primary tuberculosis. N Engl J Med (1956) 0.91
[Primary hypophosphatemic vitamin-resistant familial rickets]. Arch Fr Pediatr (1958) 0.91
[Thromboplastin formation in platelet disorders; study of 34 cases by Biggs and Douglas test]. Acta Haematol (1955) 0.90
[Not Available]. Antonie Van Leeuwenhoek (1957) 0.90
The "in vitro" heparin tolerance test in the control of dicumarol therapy. Acta Med Scand (1951) 0.90
[Willebrand-Jürgens syndrome and thrombopathies; study of 66 cases; attempt at classification]. Rev Hematol (1954) 0.90
[Heparin tolerance test in vitro in hemorrhagic syndromes and thrombosis]. Sem Hop (1950) 0.89
[Ellis-Van Creveld syndrome in a newborn dead less than a day after birth]. Arch Fr Pediatr (1952) 0.89
[Action of proteolytic enzymes on whole blood in vitro; alterations in coagulation factors and in complement]. Sem Hop (1956) 0.88
[THE CRYING CAT SYNDROME: A FURTHER CASE]. Ann Genet (1964) 0.88
[The Guillain-Barré syndrome in children; 32 case reports]. Arch Fr Pediatr (1951) 0.88
The indications for streptomycin and para-aminosalicylic acid in primary tuberculosis in children. Proc R Soc Med (1951) 0.88
[Primary tuberculosis in young children from injections]. Ann Med Interne (Paris) (1951) 0.87
[Treatment of whooping cough with the serum of hyperimmunized patients; (555 cases)]. Arch Fr Pediatr (1951) 0.87
[MORQUIO'S DISEASE. CLINICAL, RADIOLOGICAL AND BIOLOGICAL STUDY]. Presse Med (1963) 0.87
Metabolic significance of nervous symptoms due to attacks of vomiting with ketosis in children. J Pediatr (1956) 0.86
[Heparin tolerance test in vitro; hypocoagulability test, its application in diagnosis of hemorrhagic syndromes; hypercoagulability test, its application in the diagnosis of thrombosis]. Rev Hematol (1950) 0.86
[Physiopathology of hemorrhage in thrombocythemia; study of hemostasis in 27 patients]. Sang (1957) 0.86
[Congenital renal tubular insufficiency in children]. Sem Hop (1956) 0.86
[Dangers of chioramphenicol therapy; three cases of fatal hemorrhagic purpura in children]. Bull Acad Natl Med (1958) 0.86
[Preparation of a human plasmatic fraction rich in factor VIII (antihemophilic A) and poor in fibrinogen]. Nouv Rev Fr Hematol (1962) 0.86
[HERMAPHRODITISM WITH XX-XY KARYOTYPE; GENETIC STUDY OF A CASE]. Ann Genet (1964) 0.86
[FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION]. Ann Genet (1964) 0.86
[Traumatic tuberculosis in the region of the eyelid]. Arch Fr Pediatr (1951) 0.86
[Pathological variations of complement and properdin in man]. Acta Haematol (1959) 0.85
The treatment of primary tuberculosis in childhood. Pediatrics (1960) 0.85
[Fatal hemorrhagic syndromes with total incoagulability by defibrination and with fibrinolysis following abortion by injection of Javelle water; problem of defibrination in obstetrics and gynecology]. Rev Hematol (1952) 0.85
[Specific malabsorption of vitamin B12 proteinuria. Megaloblastic anemia of Imerslund-Najman-Grasbeck. Study of 4 cases]. Arch Fr Pediatr (1961) 0.85
[New data on the Hageman and P.T.A. factors and on the "contact"]. Rev Fr Etud Clin Biol (1959) 0.85
[Fetal abnormalities of rubeolar origin]. Sem Med Prof Med Soc (1956) 0.84
[New diagnostic method in hemophilia; determination of antihemophilic factors A and B]. Sang (1953) 0.84
[Glycogenosis caused by deficiency of hepatic phosphorylase]. Arch Fr Pediatr (1960) 0.84
[THE EXCRETION OF FORMIMINOGLUTAMIC ACID (FIGLU) IN THE "NORMAL" INFANT AND IN STEATORRHEA CAUSED BY DISORDER OF INTESTINAL ABSORPTION]. Rev Fr Etud Clin Biol (1964) 0.84