About: Helvetica paediatrica acta

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

journal

Attributes	Values
rdf:type	Item
description	journal (en) czasopismo naukowe (pl) revista científica (es) ساینَسی رِسالہٕ (ks) revue scientifique (fr) rivista scientifica (it) науковий журнал (uk) wissenschaftliche Fachzeitschrift (de) wetenschappelijk tijdschrift (nl)
language of work or name	wds:Q27711089-69132A0C-F162-4F00-A762-26905A4EB1A3
language of work or name	multiple languages
rdfs:label	Helvetica paediatrica acta (en) Helvetica paediatrica acta (es) Helvetica paediatrica acta (it) Helvetica paediatrica acta (nl) Helvetica paediatrica acta (ast)
skos:prefLabel	Helvetica paediatrica acta (en) Helvetica paediatrica acta (es) Helvetica paediatrica acta (it) Helvetica paediatrica acta (nl) Helvetica paediatrica acta (ast)
name	Helvetica paediatrica acta (en) Helvetica paediatrica acta (es) Helvetica paediatrica acta (it) Helvetica paediatrica acta (nl) Helvetica paediatrica acta (ast)
title	wds:Q27711089-70962E6C-6F51-4FD8-B749-AE18D36F1CD9 wds:Q27711089-C9F74CF2-160A-4389-9D26-6A10CED03A73
title	Helvetica paediatrica acta (en) Helvetica paediatrica acta (mul)
NLM Unique ID	wds:Q27711089-49BB8429-5927-4B8F-96D2-51C9BC899B05
ACNP journal ID	wds:Q27711089-131C5C9F-7E3B-4D2C-A7D6-8ECD76B55633
NLM Unique ID	0373005
ACNP journal ID	8697
instance of	wds:Q27711089-BE849AE2-231A-4656-AF80-79D679C91547
instance of	scientific journal
skos:altLabel	Helv Paediatr Acta (en)
OpenAlex ID	wds:Q27711089-42EC3A1C-12C2-4F2D-9733-540869422FF1
country of origin	wds:Q27711089-58B6B57D-F4BC-4087-9F14-3CF304B7AD21
OpenAlex ID	V2755669337
country of origin	Switzerland
Scopus source ID	wds:Q27711089-40369530-4A42-4552-828B-402DC122D2C1
ISSN	wds:Q27711089-3315BE5A-E683-4375-B2F9-A0DD78B18977
ISSN-L	wds:Q27711089-09A3DC46-78E2-4253-A5D3-6735F3E697D6
indexed in bibliographic review	wds:Q27711089-40B2D3A6-D047-4DBA-BF1A-67C16A722324
ISSN	urn:ISSN:0018-022X
ISSN-L	http://issn.org/resource/ISSN/0018-022X
Scopus source ID	37611
ISSN	0018-022X
ISSN-L	0018-022X
indexed in bibliographic review	Scopus
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q27711089
is cites work of	Cellular Immunity and Herpesvirus Infections in Cardiac-Transplant Patients Hypothalamic-pituitary dysfunction following CNS prophylaxis in acute lymphocytic leukemia: Correlation with CT scan abnormalities Congenital persistent proximal type renal tubular acidosis in two brothers Fetal anaemia in malarious areas: its causes and significance Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram syndrome). A review of 88 cases from the literature with personal observations on 3 new patients Relative underweight in cystic fibrosis and its prognostic value Epidemiology of Motor-Neuron Diseases Molecular pathology of NEU1 gene in sialidosis Inverted tandem (“mirror”) duplications in human chromosomes: Inv dup 8p, 4q, 22q Assessment of Bone Quality by Quantitative Ultrasound of Proximal Phalanges of the Hand and Fracture Rate in Children and Adolescents with Bone and Mineral Disorders Emery-dreifuss muscular dystrophy Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA Epidemiological Studies of Congenital Cytomegalovirus Infection Farber's disease as a ceramidosis: clinical, radiological and biochemical aspects Autoimmune Neutropenia Androgens and Erythropoiesis Vitamin D resistant rickets with alopecia: a form of end organ resistance to 1,25 dihydroxy vitamin D Treatment of precocious puberty with LHRH analogue in combination with cyproterone acetate-further experience Gingivo-periodontal manifestations in chronic benign neutropenia Morphological substrates of infantile spasms: studies based on surgically resected cerebral tissue Treatment of Hypoparathyroid Patients with Chlorthalidone Mucopolysaccharidosis in a Cat with Arylsulfatase B Deficiency: A Model of Maroteaux-Lamy Syndrome Two cases of phosphoenolpyruvate carboxykinase deficiency Platelet Size and Kinetics in Hereditary and Acquired Thrombocytopenia The haemolytic uraemic syndrome in childhood: A study of the long-term prognosis Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention Manipulating the Immune System with Immune Globulin Hyperinsulinism in Infancy and Childhood Laron-Type Dwarfism (Hereditary Somatomedin Deficiency): A Review Alpha-feto-protein during development and in disease Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q) Persistence of Müllerian ducts in male pseudohermaphroditism, and its relationship to cryptorchidism A female infant with duplication of chromosome 2q33 to 2q37.3 Cyclophosphamide-induced immune thrombocytopenia in a patient with ovarian carcinoma successfully treated with intravenous gamma globulin Treatment of idiopathic thrombocytic purpura in pregnancy by high-dose intravenous immunoglobulin Multiple Sclerosis in Black Children The Genetics of Hereditary Disorders of Blood Coagulation Some Unique Biologic Characteristics of the Masai of East Africa Salicylate-Induced Injury of Pyruvate-Kinase-Deficient Erythrocytes Red cell vacuoles: Their size and distribution under normal conditions and after splenectomy Evaluation of 3 hour metyrapone test in children and adolescents Prenatal Diagnosis of Cystinosis Cerebral infarction and regression of widespread aneurysms in Kawasaki's disease: case report Effect of obesity on the hypothalamo-pituitary-gonadal function in childhood Experience with human growth hormone in Great Britain: the report of the MRC Working Party Haemolytic Anaemia Associated with Glucosephosphate Isomerase (GPI) Deficiency in a Black South African Child Multiple Pterygium Syndrome type Escobar in two brothers Follow-up data from childhood to adulthood

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