Search Results - "Chemaitilly, W"

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    Bone mineral density among long-term survivors of childhood acute lymphoblastic leukemia: Results from the St. Jude Lifetime Cohort Study by Gurney, J. G., Kaste, S. C., Liu, W., Srivastava, D. K., Chemaitilly, W., Ness, K. K., Lanctot, J. Q., Ojha, R. P., Nottage, K. A., Wilson, C. L., Li, Z., Robison, L. L., Hudson, M. M.

    Published in Pediatric blood & cancer (01-07-2014)
    “…Background The prevalence of low bone mineral density (BMD) in adult survivors of childhood acute lymphoblastic leukemia (ALL), and the degree of recovery or…”
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    Journal Article
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    Disorders of glucose homeostasis in young adults treated with total body irradiation during childhood: a pilot study by Chemaitilly, W, Boulad, F, Oeffinger, K C, Sklar, C A

    Published in Bone marrow transplantation (Basingstoke) (01-09-2009)
    “…Impairment of glucose metabolism (in particular insulin resistance and type 2 diabetes mellitus) has been reported in patients who have undergone hematopoietic…”
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    Final height in pediatric patients after hyperfractionated total body irradiation and stem cell transplantation by CHEMAITILLY, W, BOULAD, F, HELLER, G, KERNAN, N. A, SMALL, T. N, O'REILLY, R. J, SKLAR, C. A

    Published in Bone marrow transplantation (Basingstoke) (01-07-2007)
    “…Impaired linear growth has been shown to occur in individuals treated during childhood with single-dose and fractionated total body irradiation (TBI) before…”
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    Metrorrhagia and precocious puberty revealing primary hypothyroidism in a child with Down’s syndrome by Chemaitilly, W, Thalassinos, C, Emond, S, Thibaud, E

    Published in Archives of disease in childhood (01-04-2003)
    “…We report a child with Down’s syndrome in whom metrorrhagia and precocious puberty revealed primary autoimmune hypothyroidism. The patient had a decreased…”
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    The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene by Chemaitilly, W, Betensky, B P, Marshall, I, Wei, J Q, Wilson, R C, New, M I

    “…The correlation of genotype to phenotype in congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency has been investigated thoroughly since the…”
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    Assessing short-statured children for growth hormone deficiency by Chemaitilly, W, Trivin, C, Souberbielle, J-C, Brauner, R

    Published in Hormone research (2003)
    “…To optimize the workup of short-statured children by defining the most appropriate tools for diagnosing growth hormone (GH) deficiency. Patients were assigned…”
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    Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1 by Thauvin-Robinet, C, El Ghouzzi, V, Chemaitilly, W, Dagoneau, N, Boute, O, Viot, G, Mégarbané, A, Sefiani, A, Munnich, A, Le Merrer, M, Cormier-Daire, V

    Published in Journal of medical genetics (01-10-2002)
    “…Dyggve-Melchior-Clausen syndrome (DMC) is an autosomal recessive condition characterised by short trunk dwarfism, scoliosis, microcephaly, coarse facies,…”
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    Adrenal insufficiency and abnormal genitalia in a 46XX female with Smith-Lemli-Opitz syndrome by Chemaitilly, W, Goldenberg, A, Baujat, G, Thibaud, E, Cormier-Daire, V, Abadie, V

    Published in Hormone research (01-01-2003)
    “…To report the first case of a 46XX female infant with Smith-Lemli-Opitz syndrome (SLOS), adrenal insufficiency and abnormal genitalia. The patient was assessed…”
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    Acute Ovarian Failure in the Childhood Cancer Survivor Study by Chemaitilly, Wassim, Mertens, Ann C., Mitby, Pauline, Whitton, John, Stovall, Marilyn, Yasui, Yutaka, Robison, Leslie L., Sklar, Charles A.

    “…Context: Defined as the loss of ovarian function within 5 yr of diagnosis, acute ovarian failure (AOF) is known to develop in a subset of survivors of…”
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    Pubertés précoces centrales des filles : prédiction de l'étiologie by Brauner, R., Couto-Silva, A.-C., Chemaitilly, W., Adan, L., Trivin, C.

    “…La puberté précoce (PP) est définie, chez la fille, par le développement des caractères sexuels avant l'âge de huit ans. La survenue d'une PP chez une fille…”
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    Central Precocious Puberty in Girls: An Evidence-Based Diagnosis Tree to Predict Central Nervous System Abnormalities by Chalumeau, Martin, Chemaitilly, Wassim, Trivin, Christine, Adan, Luis, Breart, Gerard, Brauner, Raja

    Published in Pediatrics (Evanston) (01-01-2002)
    “…To identify predictors of central precocious puberty (CPP) that reveal central nervous system (CNS) abnormalities in girls with CPP. A retrospective cohort…”
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    Central precocious puberty: clinical and laboratory features by Chemaitilly, Wassim, Trivin, Christine, Adan, Luis, Gall, Valérie, Sainte-Rose, Christian, Brauner, Raja

    Published in Clinical endocrinology (Oxford) (01-03-2001)
    “…To determine whether the initial presentation of patients with central precocious puberty (CPP) varies according to the aetiology, whether this permits the…”
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    Factors predicting adult height in girls with idiopathic central precocious puberty: implications for treatment by Adan, Luis, Chemaitilly, Wassim, Trivin, Christine, Brauner, Raja

    Published in Clinical endocrinology (Oxford) (01-03-2002)
    “…Summary objectives To optimize the indications for treating girls with idiopathic central precocious puberty with GnRH analogues, since outcomes may vary…”
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    Hypertension and adrenal disorders by Chemaitilly, Wassim, Wilson, Robert C, New, Maria I

    Published in Current hypertension reports (01-12-2003)
    “…Adrenal disorders causing hypertension can be related to the dysfunction of either the adrenal cortex or the adrenal medulla. These disorders, including…”
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    Central precocious puberty in girls: prediction of the etiology by Brauner, R, Couto-Silva, A-C, Chemaitilly, W, Adan, L, Trivin, C

    “…Precocious puberty (PP) is defined in girls by the occurrence of pubertal development before the age of 8. This development raises 3 questions: 1) Is it…”
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