False Negatives at Neonatal Screening for Congenital Adrenal Hyperplasia in Two Siblings with 21-Hydroxylase Deficiency

スポンサーリンク

概要

論文の詳細を見る

著者

関連論文

Natural pregnancy and delivery after unrelated bone marrow transplantation using fludarabine-based regimen in a Fanconi anemia patient
Secondary G-CSF Mobilized Blood Stem Cell Transplantation without Preconditioning in a Patient with Gaucher Disease : Report of a New Approach which Resulted in Complete Reversal of Severe Skeletal Involvement
Fatal adenovirus infection indistinguishable from thrombotic microangiopathy after allogeneic CD34^+ peripheral progenitor cell transplantation
Unmanipulated HLA-Haploidentical Bone Marrow Transplantation for the Treatment of Fatal, Nonmalignant Diseases in Children and Adolescents
小児期に骨髄移植を受けた患児の甲状腺機能の変化
The Kinetics of Immune Reconstitution after Cord Blood Transplantation and Selected CD34^+ Stem Cell Transplantation in Children : Comparison with Bone Marrow Transplantation
Final Height and Growth Hormone Secretion after Bone Marrow Transplantation in Children
Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
Japanese Familial Patients with Male-Limited Precocious Puberty
The Generation of Immunocompetent Dendritic Cells From CD34^+ Acute Myeloid or Lymphoid Leukemia Cells
Progressive multifocal leukoencephalopathy after allogeneic bone marrow transplantation for Wiskott-Aldrich syndrome
Clinicopathological Features of Pediatric Functional Adrenocortical Carcinoma Diagnosed by Weiss Criteria ; An Analysis of Four Cases
Expression of Transcriptional Factors of GATA4, GATA6 and SF-1 in the Developmental Process of Rat Adrenal Cortex; the Possible Contribution of GATA4 in Limited Expression before Zonal Establishment
Persistence of Mild Hyperthyrotropinemia after Discontinuation of Three-Year Course of Low-Dose L-Thyroxine Therapy in Infants with Borderline Hypothyroidism
False Negatives at Neonatal Screening for Congenital Adrenal Hyperplasia in Two Siblings with 21-Hydroxylase Deficiency
Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
Helicity Induction on a Poly(phenylacetylene) Derivative Bearing a Sulfonic Acid Pendant with Chiral Amines and Memory of the Macromolecular Helicity in Dimethyl Sulfoxide
190 CHANGES IN THYROID FUNCTION AFTER BONE MARROW TRANSPLANTATION IN YOUNG PATIENTS
47 Changes in Thyroid Function after Discontinuation of Low-dose L-Thyroxine Supplement in the Infant with Borderline Hypothyroidism
211 CONGENITAL HYPOTHYROIDISM AND APROCTIA IN AN INFANT WITH THE STRUCTURAL ABNORMALITY OF THE LONG ARM OF CHROMOSOME 15
Turner Syndrome with Ulcerative Colitis
Growth and Endocrine Function in Long-term Adult Survivors of Childhood Stem Cell Transplant

もっと見る

スポンサーリンク