Published in Arch Fr Pediatr on October 01, 1964
The human rosette-forming cell as a marker of a population of thymus-derived cells. J Clin Invest (1972) 4.80
The functions of the thymus system and the bursa system in the chicken. J Exp Med (1966) 4.07
Familial chronic muco-cutaneous candidiasis. J Med Genet (1972) 2.88
Severe combined immunodeficiency (SCID) in the mouse. Pathology, reconstitution, neoplasms. Am J Pathol (1985) 2.80
The lymphoid tissues in mice with congenital aplasia of the thymus. Clin Exp Immunol (1969) 2.77
Immune responses in congenitally thymus-less mice. I. Absence of response to oxazolone. Clin Exp Immunol (1972) 2.16
Intestinal lymphangiectasia: a protein-losing enteropathy with hypogammaglobulinemia, lymphocytopenia and impaired homograft rejection. J Clin Invest (1967) 1.88
Immunodeficiencies in chronic muco-cutaneous candidosis. Immunology (1972) 1.69
Thymic alymphoplasia. Arch Dis Child (1967) 1.27
Clinico-pathological study of thymic dysplasia. Arch Dis Child (1968) 1.25
The neonatal thymus and immune paresis. Proc R Soc Med (1968) 1.13
Restoration of T-lymphocyte deficiency with dialysable leucocyte extract. Clin Exp Immunol (1974) 1.09
Combined cellular and humoral deficiency states. Proc R Soc Med (1968) 1.06
Thymic alymphoplasia, monoclonal gammopathy, and Pneumocystis carinii pneumonia in an infant. Arch Dis Child (1968) 0.99
Granuloma formation in lymph nodes. Proc R Soc Med (1971) 0.96
Classification of immunological deficiency diseases. Proc R Soc Med (1968) 0.91
A variant of severe combined immunodeficiency with normal in vitro response to allogeneic cells and an increase in circulating B lymphocytes persisting several months after successful bone marrow graft. Clin Exp Immunol (1974) 0.85
Combined immunodeficiency with hyper-gamma-globulinaemia. Arch Dis Child (1975) 0.84
Letter: Severe combined immuno-deficiency and trisomy D. Arch Dis Child (1976) 0.78
Swiss agammaglobulinemia with hypoglycemia, osseous changes and eosinophilia. Can Med Assoc J (1970) 0.75
Role of thymus grafting in treatment of immunodeficiency. Proc R Soc Med (1975) 0.75
Genetics of immunity deficiency syndromes. J Med Genet (1970) 0.75
Immunodeficiency in children. Proc R Soc Med (1977) 0.75
The thymus, delayed hypersensitivity and autoimmunity. Proc R Soc Med (1968) 0.75
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
[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
[Diastrophic nanism]. Presse Med (1960) 1.41
[Lipomatous congenital hypoplasia of the exocrine pancreas in children. (2 cases and review of the literature)]. Arch Fr Pediatr (1961) 1.36
[Not Available]. Presse Med (1957) 1.30
[A NEW DYSOSTOSIS WITH URINARY ELIMINATION OF CHONDROITIN SULFATE B]. Presse Med (1963) 1.27
[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
[Number of dermatoglyphics in twins]. Ann Hum Genet (1957) 1.20
[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
[PROBABLE PERICENTRIC INVERSION OF THE NO. 2 CHROMOSOME AND CONGENITAL MALFORMATIONS IN A BOY]. Ann Genet (1963) 1.13
Congenital absence of beta-lipoproteins. Pediatrics (1963) 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
[Anatomical study of a case of congenital and familial multiple arthrogryposis]. Rev Obstet Ginecol Venez (1961) 1.06
[Results of an investigation of the heredity of diabetes mellitus]. Rev Fr Etud Clin Biol (1957) 1.06
TRUE HERMAPHRODITISM WITH XX-XY MOSAICISM, PROBABLY DUE TO DOUBLE FERTILIZATION OF THE OVUM. J Clin Endocrinol Metab (1965) 1.02
[Familial idiopathic acro-osteolysis; data obtained by biopsy]. Sem Hop (1959) 1.01
[Heredity of diabetes mellitus]. Journ Annu Diabetol Hotel Dieu (1961) 1.00
[GAMMA-TYPE TRANSITORY PARAPROTEINEMIA. OBSERVATION IN AN INFANT WITH ALDRICH'S SYNDROME]. Presse Med (1965) 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
[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
[Dyschondroplasia. Multiple chondromatosis of the skeleton]. Sem Hop (1960) 0.92
The genetics of pyloric stenosis. Proc R Soc Med (1953) 0.92
Genetics of haemochromatosis. Ann Hum Genet (1958) 0.92
[Acanthocytosis. Its relations to the congenital absence of beta-lipoproteins]. Presse Med (1961) 0.91
[Deletion of the short arms of chromosome 17-18: complex deformities with oligophrenia]. Arch Fr Pediatr (1963) 0.91
[Primary hypophosphatemic vitamin-resistant familial rickets]. Arch Fr Pediatr (1958) 0.91
[Not Available]. Antonie Van Leeuwenhoek (1957) 0.90
[A case of teratoma of the orbit]. Bull Soc Ophtalmol Fr (1958) 0.90
[Not Available]. Sem Hop (1958) 0.89
[Ellis-Van Creveld syndrome in a newborn dead less than a day after birth]. Arch Fr Pediatr (1952) 0.89
[Cytomegalic inclusions in adults. First French case and review of the literature]. Presse Med (1961) 0.89
[THE CRYING CAT SYNDROME: A FURTHER CASE]. Ann Genet (1964) 0.88
[MORQUIO'S DISEASE. CLINICAL, RADIOLOGICAL AND BIOLOGICAL STUDY]. Presse Med (1963) 0.87
[Primary tuberculosis in young children from injections]. Ann Med Interne (Paris) (1951) 0.87
[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
[Respiratory repercussion of thoracic rickets]. Ann Pediatr (Paris) (1960) 0.86
[A complication of intravenous therapy: giant cellular macrophagic pulmonary arteritis]. Presse Med (1960) 0.86
[Dangers of chioramphenicol therapy; three cases of fatal hemorrhagic purpura in children]. Bull Acad Natl Med (1958) 0.86
[CHRONIC LYMPHOID LEUKEMIA SECONDARILY ASSOCIATED WITH A MALIGNANT RETICULOPATHY: RICHTER'S SYNDROME]. Nouv Rev Fr Hematol (1965) 0.86
[Specific malabsorption of vitamin B12 proteinuria. Megaloblastic anemia of Imerslund-Najman-Grasbeck. Study of 4 cases]. Arch Fr Pediatr (1961) 0.85
[Lesions of myocardial fibrosis during fibrocystic disease of the pancreas]. Arch Fr Pediatr (1959) 0.85
[Fetal abnormalities of rubeolar origin]. Sem Med Prof Med Soc (1956) 0.84
[Glycogenosis caused by deficiency of hepatic phosphorylase]. Arch Fr Pediatr (1960) 0.84
[Familial dysautonomia (Riley-Day syndrome). Usual symptoms and atypical manifestations]. Arch Fr Pediatr (1961) 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
[Studies and reflections on splenoportal thromboses in children]. Arch Fr Pediatr (1961) 0.84
[Corneal opacities and metabolic disorders in Morquio's disease]. Rev Fr Etud Clin Biol (1961) 0.83
[RICHTER'S SYNDROME]. Nouv Rev Fr Hematol (1964) 0.83
[Chronic pneumopathy associated with an adenovirus infection]. Arch Fr Pediatr (1963) 0.83
[Ganglionic form of acquired toxoplasmosis in children; two case reports]. Arch Fr Pediatr (1954) 0.83
[Atypical spondylo-epiphysial dysplasia in 2 brothers]. Arch Fr Pediatr (1957) 0.83
[The severe form of idiopathic hypercalcemia; anatomo-clinical study of two cases]. Arch Fr Pediatr (1958) 0.82
[Gonadal dysgenesis with XY chromosomes. First case]. Bull Mem Soc Med Hop Paris (1960) 0.82
[Cleared cells in parenchymatous hepatitis. Comparative study by optical and electron microscopy]. Presse Med (1960) 0.82
[Early and late congenital syphilis; study of its treatment]. Sem Hop (1951) 0.81
["MESENCHYMAL CHONDROSARCOMA". APROPOS OF A CASE WITH PARA-SPINAL LOCALIZATION]. Arch Anat Pathol (Paris) (1965) 0.81
[A case of gonadal dysgenesis with normal male (XY) chromosomal formula]. Rev Fr Etud Clin Biol (1960) 0.81
[TURNER'S SYNDROME AND 47 CHROMOSOME KARYOTYPE]. Ann Genet (1963) 0.81
[KLINEFELTER'S SYNDROME IN A HYPOSPADIC INFANT. KARYOTYPE WITH 46 CHROMOSOMES]. Ann Pediatr (Paris) (1963) 0.81
[Not Available]. Sem Hop (1958) 0.81
[Pseudo-myopathic form varicella causing polyradiculoneuritis]. Arch Fr Pediatr (1952) 0.81
[Apropos of a recent case of Budd-Chiari syndrome]. Presse Med (1960) 0.81
[Essential cysts of long bones; anatomo-pathological study & surgical therapy]. Rev Chir Orthop Reparatrice Appar Mot (1958) 0.81
[Fatal Candida infections in newborn and in infants; anatomical and histological aspects of 6 cases]. Sem Hop (1958) 0.80
[Bullous erythroderma with epidermolysis]. Presse Med (1963) 0.80
[FAMILIAL TURNER'S SYNDROME. STUDY OF 2 FAMILIES WITH XO AND XX KARYOTYPES]. Ann Pediatr (Paris) (1963) 0.80
XX/XO mosaics in Turner's syndrome. Two further cases. Lancet (1961) 0.80
[Study in cellular culture of Mengo encephalomyelitis virus]. Ann Inst Pasteur (Paris) (1955) 0.80
[HEPATO-RENAL POLYCYSTIC DISEASES]. Rev Int Hepatol (1964) 0.79
Studies on combined adsorbed poliomyelitis-DTP vaccine. Poliomyelitis antibody responses of children to primary immunization. Acta Paediatr (1962) 0.79
[Maternal age and the birth order in a sample of twins]. Acta Genet Stat Med (1955) 0.78
[Congenital absence of beta-lipoproteins: study of fat absorption after exsanguinotransfusion measuring the half-life of injected beta-lipoproteins]. Rev Fr Etud Clin Biol (1961) 0.78
[Study of karyotypes in Stein-Leventhal syndrome]. Ann Endocrinol (Paris) (1962) 0.78
[RUBELLA IN THE PREGNANT WOMAN]. Arch Gesamte Virusforsch (1965) 0.78
[Case of aneurysm of the splenic artery with splenomegaly and portal hypertension]. Mem Acad Chir (Paris) (1955) 0.77