عنوان ترانسليتريتد: Tratamiento con Hormona de Crecimiento en pacientes con déficit de hormona de crecimiento, talla baja idiopática, mutación gen SHOX, pequeños para edad gestacional y síndrome de Turner.

المؤلفون: Griffero González M; Hospital Luis Calvo Mackenna, Santiago, Chile., González Navarrete D; Universidad de Santiago de Chile, Santiago, Chile., Tolosa Navarro F; Hospital Clínico San Borja Arriarán, Santiago, Chile., López Cuevas P; Instituto de Investigaciones Materno Infantil, Hospital Clínico San Borja Arriarán, Santiago, Chile., Rodríguez Convertino F; Instituto de Investigaciones Materno Infantil, Hospital Clínico San Borja Arriarán, Santiago, Chile., Román Reyes R; Instituto de Investigaciones Materno Infantil, Hospital Clínico San Borja Arriarán, Santiago, Chile.

المصدر: Andes pediatrica : revista Chilena de pediatria [Andes Pediatr] 2024 Apr; Vol. 95 (2), pp. 151-158. Date of Electronic Publication: 2024 Apr 13.

نوع المنشور: Journal Article; English Abstract

بيانات الدورية: Publisher: Sociedad Chilena de Pediatría Country of Publication: Chile NLM ID: 101778868 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2452-6053 (Electronic) Linking ISSN: 24526045 NLM ISO Abbreviation: Andes Pediatr Subsets: MEDLINE

مواضيع طبية MeSH: Short Stature Homeobox Protein*/genetics , Turner Syndrome*/drug therapy , Turner Syndrome*/genetics , Human Growth Hormone*/therapeutic use , Infant, Small for Gestational Age* , Body Height* , Growth Disorders*/genetics , Growth Disorders*/drug therapy , Mutation*, Humans ; Female ; Retrospective Studies ; Male ; Child ; Child, Preschool ; Adolescent ; Treatment Outcome ; Infant ; Haploinsufficiency

المؤلفون: Hattori A; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.; Division of Diversity Research, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Seki A; Department of Orthopaedic Surgery, National Medical Center for Children and Mothers, Tokyo, 157-8535, Japan., Inaba N; Department of Orthopaedic Surgery, National Medical Center for Children and Mothers, Tokyo, 157-8535, Japan., Nakabayashi K; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Takeda K; Department of Allergy and Clinical Immunology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Tatsusmi K; Center for Regenerative Medicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Naiki Y; Division of Endocrinology and Metabolism, National Medical Center for Children and Mothers, Tokyo, 157-8535, Japan., Nakamura A; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Ishiwata K; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Matsumoto K; Department of Allergy and Clinical Immunology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Nasu M; Center for Regenerative Medicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Okamura K; Department of Systems BioMedicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Michigami T; Department of Bone and Mineral Research, Research Institute, Osaka Women's and Children's Hospital, Osaka Prefectural Hospital Organization, Izumi, 594-1101, Japan., Katoh-Fukui Y; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Umezawa A; Center for Regenerative Medicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Ogata T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, 431-3192, Japan.; Department of Pediatrics, Hamamatsu Medical Center, Hamamatsu, 432-8580, Japan., Kagami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan., Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan. fukami-m@ncchd.go.jp.; Division of Diversity Research, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan. fukami-m@ncchd.go.jp.

المصدر: Scientific reports [Sci Rep] 2024 Apr 05; Vol. 14 (1), pp. 8069. Date of Electronic Publication: 2024 Apr 05.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

مواضيع طبية MeSH: Chondrocytes*/metabolism , Homeodomain Proteins*/genetics, Child ; Adult ; Humans ; Male ; Female ; Short Stature Homeobox Protein/genetics ; DNA Methylation ; Epigenesis, Genetic ; Cartilage/metabolism

المؤلفون: Srivastava P; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Tyagi A; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Bamba C; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Kumari A; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Kaur H; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Child Growth and Anthropology Unit, Chandigarh, India, Seth S; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Kaur A; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Panigrahi I; Advanced Pediatrics Centre (APC), Postgraduate Institute of Medical Education & Research (PGIMER), Genetic Metabolic Unit, Chandigarh, India, Dayal D; Advanced Pediatrics Centre, Postgraduate Institute of Medical Education & Research (PGIMER), Pediatric Endocrinology Unit, Chandigarh, India, Pramanik S; IPGMER and SSKM Hospital, Clinic of Endocrinology, Kolkata, India, Mandal K; Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Department of Medical Genetics, Lucknow, India

المصدر: Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2024 Mar 11; Vol. 16 (1), pp. 41-49. Date of Electronic Publication: 2023 Sep 26.

نوع المنشور: Meta-Analysis; Review; Journal Article

بيانات الدورية: Publisher: Galenos Yayınevi Country of Publication: Turkey NLM ID: 101519456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1308-5735 (Electronic) NLM ISO Abbreviation: J Clin Res Pediatr Endocrinol Subsets: MEDLINE

مواضيع طبية MeSH: Dwarfism*/epidemiology , Dwarfism*/genetics , Osteochondrodysplasias*/genetics, Child ; Female ; Humans ; Genes, Homeobox ; Homeodomain Proteins/genetics ; Short Stature Homeobox Protein/genetics ; Growth Disorders/epidemiology ; Growth Disorders/genetics ; India/epidemiology

المؤلفون: Seiersen KV; Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark. Electronic address: kvs@clin.au.dk., Henriksen TB; Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark., Andelius TCK; Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark., Andreasen L; Department of Clinical Genetics, Aarhus University Hospital, Denmark., Diemer T; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark., Gudmundsdottir G; Department of Neurosurgery, Aarhus University Hospital, Denmark., Vogel I; Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark; Department of Clinical Genetics, Aarhus University Hospital, Denmark; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark., Gjørup V; Department of Gynaecology and Obstetrics, Aarhus University Hospital, Aarhus, Denmark., Gregersen PA; Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark; Department of Clinical Genetics, Aarhus University Hospital, Denmark; Centre for Rare Diseases, Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.

المصدر: European journal of medical genetics [Eur J Med Genet] 2024 Feb; Vol. 67, pp. 104894. Date of Electronic Publication: 2023 Dec 07.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Achondroplasia*/genetics , Osteochondrodysplasias*/genetics, Female ; Humans ; Infant ; Denmark ; Gene Deletion ; Genes, Homeobox ; Growth Disorders/genetics ; Homeodomain Proteins/genetics ; Short Stature Homeobox Protein/genetics

المؤلفون: Spurná Z; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Čapková P; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic. Electronic address: Pavlina.Capkova@fnol.cz., Punová L; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., DuchoslavovÁ J; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Aleksijevic D; Paediatrics Department, Palacký University and University Hospital, Olomouc, Czech Republic., Venháčová P; Paediatrics Department, Palacký University and University Hospital, Olomouc, Czech Republic., Srovnal J; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic; Institute of Molecular and Translational Medicine, Czech Advanced Technology and Research Institute, Palacky University in Olomouc, Czech Republic; Cancer Research Czech Republic, Olomouc, Czech Republic., Štellmachová J; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Curtisová V; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Bitnerová V; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Petřková J; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; First Department of Internal Medicine - Cardiology, University Hospital Olomouc, Olomouc, Czech Republic; First Department of Internal Medicine - Cardiology, Palacký University in Olomouc, Olomouc, Czech Republic; Institute of Pathological Physiology, Palacký University in Olomouc, Olomouc, Czech Republic., Kolaříková K; Department of Neurology, University Hospital Olomouc, Czech Republic; Department of Neurology, Palacky University Olomouc, Czech Republic., Janíková M; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic; Institute of Clinical and Molecular Pathology, Palacký University in Olomouc, Olomouc, Czech Republic., Kratochvílová R; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic., Vrtěl P; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Vodička R; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Vrtěl R; Institute of Medical Genetics, Olomouc University Hospital, Olomouc, Czech Republic; Institute of Medical Genetics, Palacký University in Olomouc, Olomouc, Czech Republic., Zapletalová J; Paediatrics Department, Palacký University and University Hospital, Olomouc, Czech Republic.

المصدر: Gene [Gene] 2024 Jan 20; Vol. 892, pp. 147881. Date of Electronic Publication: 2023 Oct 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE

مواضيع طبية MeSH: Growth Disorders*/epidemiology , Growth Disorders*/genetics , Growth Disorders*/metabolism , Skeleton*/metabolism, Child ; Humans ; Czech Republic ; Genetic Association Studies ; Gene Frequency/genetics ; Short Stature Homeobox Protein/genetics

المؤلفون: Toni L; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Plachy L; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Dusatkova P; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Amaratunga SA; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Elblova L; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Sumnik Z; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Kolouskova S; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Snajderova M; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Obermannova B; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Pruhova S; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia., Lebl J; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czechia.

المصدر: Hormone research in paediatrics [Horm Res Paediatr] 2024; Vol. 97 (1), pp. 40-52. Date of Electronic Publication: 2023 Apr 05.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 101525157 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1663-2826 (Electronic) Linking ISSN: 16632818 NLM ISO Abbreviation: Horm Res Paediatr Subsets: MEDLINE

مواضيع طبية MeSH: Silver-Russell Syndrome*/genetics , Dwarfism* , Human Growth Hormone*/genetics, Child ; Infant, Newborn ; Humans ; Insulin-Like Growth Factor I ; Growth Disorders/genetics ; Growth Disorders/diagnosis ; Gestational Age ; Infant, Small for Gestational Age ; Body Height/genetics ; Short Stature Homeobox Protein

المؤلفون: Gu L; Prenatal Diagnosis Center, Center of Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, Jiangsu 210008, China. jie1967@126.com., Liu W, Zhu X, Li J

المصدر: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2024 Feb 10; Vol. 41 (2), pp. 205-208.

نوع المنشور: English Abstract; Journal Article

بيانات الدورية: Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print ISSN: 1003-9406 (Print) Linking ISSN: 10039406 NLM ISO Abbreviation: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Subsets: MEDLINE

مواضيع طبية MeSH: Prenatal Diagnosis*/methods , Chromosome Disorders*/genetics, Pregnancy ; Female ; Humans ; Chromosome Aberrations ; Phenotype ; Fetus ; Short Stature Homeobox Protein/genetics

المؤلفون: Jouira, Ghada, Rebai, Haithem, Alexe, Dan Iulian, Sahli, Sonia

المصدر: Adapted Physical Activity Quarterly; Jul2024, Vol. 41 Issue 3, p382-401, 20p

مصطلحات موضوعية: EXERCISE physiology, MOTOR ability, THERAPEUTICS, PLYOMETRICS, BODY mass index, DATA analysis, HUMAN services programs, STATISTICAL sampling, BODY weight, QUESTIONNAIRES, EVALUATION of human services programs, PHYSICAL training & conditioning, RANDOMIZED controlled trials, AGE distribution, DESCRIPTIVE statistics, STRENGTH training, STATURE, CONTROL groups, PRE-tests & post-tests, STATISTICS, ANALYSIS of variance, BODY movement, ATHLETIC ability, EXERCISE tests, JUMPING, COMPARATIVE studies, CONFIDENCE intervals, DATA analysis software, SPRINTING, POSTURAL balance

المؤلفون: Cai M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China., Chen X; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China., Li Y; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China., Lin N; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China., Huang H; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China., Xu L; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, P.R. China.

المصدر: Journal of perinatal medicine [J Perinat Med] 2023 Oct 18; Vol. 52 (1), pp. 96-101. Date of Electronic Publication: 2023 Oct 18 (Print Publication: 2024).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Walter De Gruyter Country of Publication: Germany NLM ID: 0361031 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 1619-3997 (Electronic) Linking ISSN: 03005577 NLM ISO Abbreviation: J Perinat Med Subsets: MEDLINE

مواضيع طبية MeSH: Pregnancy Outcome* , Prenatal Diagnosis*, Child ; Adult ; Infant ; Humans ; Pregnancy ; Female ; Ultrasonography ; Phenotype ; Fetus ; Short Stature Homeobox Protein/genetics

Personal Name: Hatch, Isaiah A. 1831-. Songs and music, Hatch, Isaiah A. 1831-.

الموضوعات: Broadsides 19th century. United States, Songs Texts. 19th century United States, Popular music Texts. 19th century United States, Sacred songs Texts., Memorials Songs and music Texts., Death Songs and music Texts., Stature Songs and music Texts., Musique populaire Textes. 19e siècle États-Unis, Chants sacrés Textes., Broadsides., Death., Memorials., Popular music., Sacred songs., Songs., Stature., United States.

مصطلحات الفهرس: Music Texts., Texts.

URL: http://worldcat.org/oclc/60777103/viewonline