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1دورية أكاديمية
المؤلفون: Black WR, Jones JT, Rush ET, Malloy Walton L, Harding A
المصدر: Journal of Multidisciplinary Healthcare, Vol Volume 16, Pp 191-195 (2023)
مصطلحات موضوعية: ehlers-danlos, hypermobility, multidisciplinary, pediatrics, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Rush ET, Schaefer GB
المصدر: Seminars in Pediatric Neurology; Mar2010, Vol. 17 Issue 1, p51-53, 3p
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3
المؤلفون: Mullegama SV, Kiernan KA, Torti E, Pavlovsky E, Tilton N, Sekula A, Gao H, Alaimo JT, Engleman K, Rush ET, Blocker K, Dipple KM, Fettig VM, Hare H, Glass I, Grange DK, Griffin M, Phornphutkul C, Massingham L, Mehta L, Miller DE, Thies J, Merritt JL 2nd, Muller E 2nd, Osmond M, Sawyer SL, Slaugh R, Hickey RE, Wolf B, Choudhary S, Simonović M, Zhang Y, Palculict TB, Telegrafi A, Carere DA, Wentzensen IM, Morrow MM, Monaghan KG, Juusola J, Yang J
مؤلفون مشاركون: Care4Rare Canada Consortium, Undiagnosed Diseases Network
المصدر: American journal of human genetics [Am J Hum Genet] 2024 Jun 06; Vol. 111 (6), pp. 1240. Date of Electronic Publication: 2024 May 14.
نوع المنشور: Published Erratum
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: PubMed not MEDLINE; MEDLINE
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4دورية أكاديمية
المؤلفون: Dahir KM; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, 1215 21st Ave S Suite 8210, Nashville, TN, 37232, USA. kathryn.dahir@vumc.org., Rush ET; Division of Clinical Genetics, Children's Mercy Kansas City, 2401 Gillham Rd, Kansas City, MO, 64108, USA. etrush@cmh.edu.; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA. etrush@cmh.edu.; Department of Internal Medicine, University of Kansas School of Medicine, Kansas City, KS, USA. etrush@cmh.edu., Diaz-Mendoza S; OPEN Health Group, Marlow, UK., Kishnani PS; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
المصدر: Journal of endocrinological investigation [J Endocrinol Invest] 2024 Jun; Vol. 47 (6), pp. 1487-1497. Date of Electronic Publication: 2024 Jan 18.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Springer Country of Publication: Italy NLM ID: 7806594 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1720-8386 (Electronic) Linking ISSN: 03914097 NLM ISO Abbreviation: J Endocrinol Invest Subsets: MEDLINE
مواضيع طبية MeSH: Hypophosphatasia*/diagnosis , Delphi Technique* , Disease Progression* , Consensus* , Severity of Illness Index*, Humans ; Adult ; United States/epidemiology ; Female ; Male ; Health Personnel ; Surveys and Questionnaires
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5دورية أكاديمية
المؤلفون: McNeill HC; Faculty Affairs and Development, Children's Mercy Kansas City, 2401 Gillham Road, Kansas City, MO, 64108, USA. hcmcneill@cmh.edu., Hill JD; Faculty Affairs and Development, Children's Mercy Kansas City, 2401 Gillham Road, Kansas City, MO, 64108, USA.; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA.; Department of Population Health, School of Medicine, University of Kansas, Kansas City, KS, USA., Chandler M; Faculty Affairs and Development, Children's Mercy Kansas City, 2401 Gillham Road, Kansas City, MO, 64108, USA., Rush ET; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA.; Faculty Affairs and Development, Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.; Department of Internal Medicine, School of Medicine, University of Kansas, Kansas City, KS, USA., Montello M; Faculty Affairs and Development, Children's Mercy Kansas City, 2401 Gillham Road, Kansas City, MO, 64108, USA.
المصدر: Journal of clinical psychology in medical settings [J Clin Psychol Med Settings] 2024 May 18. Date of Electronic Publication: 2024 May 18.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Springer Country of Publication: United States NLM ID: 9435680 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-3572 (Electronic) Linking ISSN: 10689583 NLM ISO Abbreviation: J Clin Psychol Med Settings Subsets: MEDLINE
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6دورية أكاديمية
المؤلفون: Dahir KM; Endocrinology and Diabetes, Vanderbilt University Medical Center, Nashville, TN 37232, United States., Ing SW; Division of Endocrinology, Diabetes, and Metabolism, Wexner Medical Center, Ohio State University, Columbus, OH 43210, United States., Deal C; Department of Rheumatology, Center for Osteoporosis and Metabolic Bone Disease, Cleveland Clinic, Cleveland, OH 44195, United States., Messali A; Health Economics and Outcomes Research (AM) and Medical Affairs (CD), Alexion, AstraZeneca Rare Disease, Boston, MA 02210, United States., Bates T; Health Economics and Outcomes Research (AM) and Medical Affairs (CD), Alexion, AstraZeneca Rare Disease, Boston, MA 02210, United States., Rush ET; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO 64108, United States.; Department of Pediatrics, University of Missouri - Kansas City School of Medicine, Kansas City, MO 64108, United States.
المصدر: JBMR plus [JBMR Plus] 2024 May 07; Vol. 8 (8), pp. ziae062. Date of Electronic Publication: 2024 May 07 (Print Publication: 2024).
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 101707013 Publication Model: eCollection Cited Medium: Internet ISSN: 2473-4039 (Electronic) Linking ISSN: 24734039 NLM ISO Abbreviation: JBMR Plus Subsets: PubMed not MEDLINE
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7
المؤلفون: Khan AA; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada. aliya@mcmaster.ca., Brandi ML; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy.; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy., Rush ET; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.; Division of Endocrinology, Metabolism, Osteoporosis and Genetics, Department of Internal Medicine, University of Kansas School of Medicine, Kansas City, KS, USA.; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA., Ali DS; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Al-Alwani H; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Almonaei K; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Alsarraf F; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Bacrot S; Department of Genetics, Centre Hospitalier de Versailles, Hôpital André Mignot, Versailles, France., Dahir KM; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Dandurand K; Department of Medicine, Endocrinology and Metabolism, Université de Sherbrooke, Sherbrooke, QC, Canada., Deal C; Center for Osteoporosis and Metabolic Bone Disease, Department of Rheumatology, The Cleveland Clinic Foundation, Cleveland, OH, USA., Ferrari SL; Division of Bone Diseases, Department of Internal Medicine Specialties, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland., Giusti F; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy., Guyatt G; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Hatcher E; Neuromuscular Clinic, McMaster University Medical Centre, Hamilton Health Sciences, Hamilton, Canada., Ing SW; Division of Endocrinology, Diabetes & Metabolism, Ohio State University Wexner Medical Center, Columbus, OH, USA., Javaid MK; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK., Khan S; Bone Research and Education Centre, Oakville, ON, Canada., Kocijan R; Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of OEGK and AUVA, Trauma Centre Meidling, 1St Medical Department Hanusch Hospital, 1140, Vienna, Austria., Linglart A; APHP, Bicêtre Paris-Sud, UniversityParis Sud, Paris-Saclay, Le Kremlin Bicêtre, Paris, France., M'Hiri I; Bone Research and Education Centre, Oakville, ON, Canada., Marini F; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy., Nunes ME; Division of Medical Genetics and Metabolism, Valley Children's HealthCare, Madera, CA, USA., Rockman-Greenberg C; Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB, Canada., Roux C; INSERM CRESS UMR 1153, Paris, France.; Department of Rheumatology, APHP-Centre, Cochin Hospital, Université Paris-Cité, Paris, France., Seefried L; Musculoskeletal Center Wuerzburg, University of Würzburg, Würzburg, Germany., Simmons JH; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Starling SR; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA., Ward LM; Children's Hospital of Eastern Ontario, Department of Pediatrics, University of Ottawa, Ottawa, ON, Canada., Yao L; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Brignardello-Petersen R; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Michael Lewiecki E; New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM, USA.
المصدر: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA [Osteoporos Int] 2024 May; Vol. 35 (5), pp. 933-934.
نوع المنشور: Published Erratum
بيانات الدورية: Publisher: Springer International Country of Publication: England NLM ID: 9100105 Publication Model: Print Cited Medium: Internet ISSN: 1433-2965 (Electronic) Linking ISSN: 0937941X NLM ISO Abbreviation: Osteoporos Int Subsets: PubMed not MEDLINE; MEDLINE
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8دورية أكاديمية
المؤلفون: Brandi ML; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy. marialuisa.brandi@unifi.it.; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy. marialuisa.brandi@unifi.it., Khan AA; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Rush ET; Division of Clinical Genetics, Children's Mercy Kansas City and Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA.; Division of Endocrinology, Metabolism, Osteoporosis, and Genetics, Department of Internal Medicine, University of Kansas School of Medicine, Kansas City, KS, USA., Ali DS; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Al-Alwani H; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Almonaei K; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Alsarraf F; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Bacrot S; Department of Genetics, Centre Hospitalier de Versailles, Hôpital André Mignot, Versailles, France., Dahir KM; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Dandurand K; Department of Medicine, Endocrinology and Metabolism, Université de Sherbrooke, Sherbrooke, QC, Canada., Deal C; Center for Osteoporosis and Metabolic Bone Disease, Department of Rheumatology, The Cleveland Clinic Foundation, Cleveland, OH, USA., Ferrari SL; Division of Bone Diseases, Department of Internal Medicine Specialties, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland., Giusti F; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy., Guyatt G; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada., Hatcher E; Neuromuscular Clinic, McMaster University Medical Centre, Hamilton Health Sciences, Hamilton, ON, Canada., Ing SW; Division of Endocrinology, Diabetes, & Metabolism, Ohio State University Wexner Medical Center, Columbus, OH, USA., Javaid MK; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK., Khan S; Bone Research and Education Centre, Oakville, ON, Canada., Kocijan R; Trauma Centre Meidling, Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of OEGK and AUVA, 1St Medical Department Hanusch Hospital, 1140, Vienna, Austria., Lewiecki EM; New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM, USA., Linglart A; APHP, Bicêtre Paris-Sud, University Paris Sud, Paris-Saclay, Le Kremlin Bicêtre, Paris, France., M'Hiri I; Bone Research and Education Centre, Oakville, ON, Canada., Marini F; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy., Nunes ME; Division of Medical Genetics and Metabolism, Valley Children's HealthCare, Madera, CA, USA., Rockman-Greenberg C; Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB, Canada., Seefried L; Musculoskeletal Center Würzburg, University of Würzburg, Würzburg, Germany., Simmons JH; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Starling SR; Division of Clinical Genetics, Children's Mercy Kansas City and Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA., Ward LM; Department of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada., Yao L; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada., Brignardello-Petersen R; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada., Roux C; INSERM CRESS UMR 1153, Paris, France.; Université Paris-Cité, Department of Rheumatology, APHP-Centre, Cochin Hospital, Paris, France.
المصدر: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA [Osteoporos Int] 2024 Mar; Vol. 35 (3), pp. 439-449. Date of Electronic Publication: 2023 Nov 20.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Springer International Country of Publication: England NLM ID: 9100105 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1433-2965 (Electronic) Linking ISSN: 0937941X NLM ISO Abbreviation: Osteoporos Int Subsets: MEDLINE
مواضيع طبية MeSH: Hypophosphatasia*/diagnosis , Hypophosphatasia*/epidemiology , Hypophosphatasia*/genetics, Infant ; Adult ; Infant, Newborn ; Humans ; Alkaline Phosphatase/genetics ; Mutation ; Prevalence
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9دورية أكاديمية
المؤلفون: Khan AA; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada. aliya@mcmaster.ca., Brandi ML; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy.; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy., Rush ET; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.; Division of Endocrinology, Metabolism, Osteoporosis and Genetics, Department of Internal Medicine, University of Kansas School of Medicine, Kansas City, KS, USA.; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA., Ali DS; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Al-Alwani H; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Almonaei K; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Alsarraf F; Division of Endocrinology and Metabolism, McMaster University, Hamilton, Canada., Bacrot S; Department of Genetics, Centre Hospitalier de Versailles, Hôpital André Mignot, Versailles, France., Dahir KM; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Dandurand K; Department of Medicine, Endocrinology and Metabolism, Université de Sherbrooke, Sherbrooke, QC, Canada., Deal C; Center for Osteoporosis and Metabolic Bone Disease, Department of Rheumatology, The Cleveland Clinic Foundation, Cleveland, OH, USA., Ferrari SL; Division of Bone Diseases, Department of Internal Medicine Specialties, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland., Giusti F; Donatello Bone Clinic, Villa Donatello Hospital, Florence, Italy., Guyatt G; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Hatcher E; Neuromuscular Clinic, McMaster University Medical Centre, Hamilton Health Sciences, Hamilton, Canada., Ing SW; Division of Endocrinology, Diabetes & Metabolism, Ohio State University Wexner Medical Center, Columbus, OH, USA., Javaid MK; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK., Khan S; Bone Research and Education Centre, Oakville, ON, Canada., Kocijan R; Ludwig Boltzmann Institute of Osteology at Hanusch Hospital of OEGK and AUVA, Trauma Centre Meidling, 1St Medical Department Hanusch Hospital, 1140, Vienna, Austria., Linglart A; APHP, Bicêtre Paris-Sud, UniversityParis Sud, Paris-Saclay, Le Kremlin Bicêtre, Paris, France., M'Hiri I; Bone Research and Education Centre, Oakville, ON, Canada., Marini F; F.I.R.M.O. Italian Foundation for the Research On Bone Diseases, Florence, Italy., Nunes ME; Division of Medical Genetics and Metabolism, Valley Children's HealthCare, Madera, CA, USA., Rockman-Greenberg C; Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB, Canada., Roux C; INSERM CRESS UMR 1153, Paris, France.; Université Paris-Cité, Department of Rheumatology, APHP-Centre, Cochin Hospital, Paris, France., Seefried L; Musculoskeletal Center Wuerzburg, University of Würzburg, Würzburg, Germany., Simmons JH; Division of Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA., Starling SR; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA., Ward LM; Children's Hospital of Eastern Ontario, Department of Pediatrics, University of Ottawa, Ottawa, ON, Canada., Yao L; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Brignardello-Petersen R; Department of Health Research Methods, Evidence and Impact at McMaster University, Hamilton, Canada., Lewiecki EM; New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM, USA.
المصدر: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA [Osteoporos Int] 2024 Mar; Vol. 35 (3), pp. 431-438. Date of Electronic Publication: 2023 Nov 20.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Springer International Country of Publication: England NLM ID: 9100105 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1433-2965 (Electronic) Linking ISSN: 0937941X NLM ISO Abbreviation: Osteoporos Int Subsets: MEDLINE
مواضيع طبية MeSH: Hypophosphatasia*/diagnosis , Hypophosphatasia*/genetics, Adult ; Child ; Humans ; Mutation ; Retrospective Studies ; Alkaline Phosphatase/genetics ; Genotype ; Phenotype
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10دورية أكاديمية
المؤلفون: Farman MR; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Rehder C; Duke University Medical Center, Department of Pathology, Durham, USA., Malli T; Laboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria., Rockman-Greenberg C; Department of Pediatrics and Child Health Max Rady College of Medicine, Rady Faculty of Health Sciences, Winnipeg, Canada., Dahir K; Vanderbilt University Medical Center, Program for Metabolic Bone Disorders, Nashville, TN, USA., Martos-Moreno GÁ; Departments of Pediatrics & Pediatric Endocrinology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain; Department of Pediatrics, Universidad Autónoma de Madrid, Madrid, Spain; CIBER Fisiopatología de la Obesidad y Nutrición, ISCIII, Madrid, Spain, Linglart A; AP-HP, Paris Saclay University, INSERM, Bicêtre Paris Saclay hospital, Le Kremlin-Bicêtre, France, Ozono K; Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan, Seefried L; Julius-Maximilian University, Würzburg, Germany., Del Angel G; Alexion, AstraZeneca Rare Disease, Boston, MA, USA, Webersinke G; Laboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria., Barbazza F; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., John LK; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Delana Mudiyanselage SMA; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Högler F; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Nading EB; Duke University Medical Center, Division of Medical Genetics, Department of Pediatrics, Durham, USA, Huggins E; Duke University Medical Center, Division of Medical Genetics, Department of Pediatrics, Durham, USA, Rush ET; Division of Clinical Genetics, Children's Mercy Hospital Kansas City, Kansas City, MO, USA; Department of Internal Medicine, University of Kansas School of Medicine, Kansas City, KS, USA; Department of Pediatrics, University of Missouri – Kansas City School of Medicine, Kansas City, MO, USA, El-Gazzar A; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Kishnani PS; Duke University Medical Center, Division of Medical Genetics, Department of Pediatrics, Durham, USA, Högler W; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
المصدر: Bone [Bone] 2024 Jan; Vol. 178, pp. 116947. Date of Electronic Publication: 2023 Oct 26.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Elsevier Science Country of Publication: United States NLM ID: 8504048 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2763 (Electronic) Linking ISSN: 18732763 NLM ISO Abbreviation: Bone Subsets: MEDLINE
مواضيع طبية MeSH: Alkaline Phosphatase*/genetics , Alkaline Phosphatase*/chemistry , Hypophosphatasia*/genetics , Hypophosphatasia*/pathology, Humans ; Mutation/genetics ; Artificial Intelligence ; Delayed Diagnosis