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1. Full Text Updated Clinical Classification of Pulmonary Hypertension
by Simonneau, Gerald, MD and Gatzoulis, Michael A., MD, PhD and Adatia, Ian, MD and Celermajer, David, MD, PhD and Denton, Chris, MD, PhD and Ghofrani, Ardeschir, MD and Gomez Sanchez, Miguel Angel, MD and Krishna Kumar, R., MD and Landzberg, Michael, MD and Machado, Roberto F., MD and Olschewski, Horst, MD and Robbins, Ivan M., MD and Souza, Rogiero, MD, PhD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2013, Volume 62, Issue 25, pp. D34 - D41
In 1998, a clinical classification of pulmonary hypertension (PH) was established, categorizing PH into groups which share similar pathological and hemodynamic... 
Cardiovascular | Internal Medicine | chronic thromboembolic pulmonary hypertension | PH due to chronic lung diseases | PH due to left heart disease | pulmonary arterial hypertension | pulmonary hypertension | SURVIVAL | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK | PREVALENCE | SYSTEMIC-SCLEROSIS | PORTOPULMONARY HYPERTENSION | SEROTONIN-REUPTAKE INHIBITORS | CONGENITAL HEART-DISEASE | ARTERIAL-HYPERTENSION | SICKLE-CELL-DISEASE | Anemia, Hemolytic - classification | Heart Defects, Congenital - classification | Hypertension, Pulmonary - diagnosis | Hypertension, Pulmonary - classification | Connective Tissue Diseases - classification | Connective Tissue Diseases - epidemiology | Humans | Connective Tissue Diseases - diagnosis | Hypertension, Pulmonary - epidemiology | Animals | Anemia, Hemolytic - diagnosis | Heart Defects, Congenital - epidemiology | Heart Defects, Congenital - diagnosis | Anemia, Hemolytic - epidemiology | Medical colleges | Genetic disorders | Anemia | Pulmonary hypertension
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2. Full Text Updated Clinical Classification of Pulmonary Hypertension
by Simonneau, Gérald, MD and Robbins, Ivan M., MD and Beghetti, Maurice, MD and Channick, Richard N., MD and Delcroix, Marion, MD, PhD and Denton, Christopher P., MD, PhD and Elliott, C. Gregory, MD and Gaine, Sean P., MD, PhD and Gladwin, Mark T., MD and Jing, Zhi-Cheng, MD and Krowka, Michael J., MD and Langleben, David, MD and Nakanishi, Norifumi, MD, PhD and Souza, Rogério, MD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2009, Volume 54, Issue 1, pp. S43 - S54
The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in... 
Cardiovascular | Internal Medicine | clinical classification | pulmonary arterial hypertension | pulmonary hypertension | VENOOCCLUSIVE-DISEASE | CHRONIC HEART-FAILURE | CARDIAC & CARDIOVASCULAR SYSTEMS | HEREDITARY HEMORRHAGIC TELANGIECTASIA | CONNECTIVE-TISSUE-DISEASE | SYSTEMIC-SCLEROSIS | INTERSTITIAL LUNG-DISEASE | GLYCOGEN-STORAGE-DISEASE | ARTERIAL-HYPERTENSION | SICKLE-CELL-DISEASE | OF-THE-LITERATURE | Hypertension, Pulmonary - classification | Prognosis | Comorbidity | Humans | Calcium Channel Blockers - therapeutic use | Antihypertensive Agents - administration & dosage | Anticoagulants - therapeutic use | Treatment Outcome | Hypertension, Pulmonary - epidemiology | Evidence-Based Medicine | Scleroderma, Systemic - epidemiology | Randomized Controlled Trials as Topic | Algorithms | Hypertension, Pulmonary - drug therapy | Endothelin Receptor Antagonists | Epoprostenol - administration & dosage | Hypertension | Medical colleges | Micropollutants | Sickle cell anemia | Architecture | Respiratory agents | Congenital heart disease | HIV (Viruses) | Peptide hormones | Coronary heart disease | Gene mutations | Bone morphogenetic proteins | Kidney diseases | Cardiology | Health aspects | Personal video recorders | Anemia | Pulmonary hypertension | Genetic counseling | Surgery | Classification | Clinical trials | Cardiovascular disease | Mutation | Family medical history | Drug therapy | Defects
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3. Full Text Clinical classification of pulmonary hypertension
by Simonneau, Gerald and Galiè, Nazzareno and Rubin, Lewis J and Langleben, David and Seeger, Werner and Domenighetti, Guido and Gibbs, Simon and Lebrec, Didier and Speich, Rudolf and Beghetti, Maurice and Rich, Stuart and Fishman, Alfred
Journal of the American College of Cardiology, ISSN 0735-1097, 06/2004, Volume 43, Issue 12, pp. S5 - S12
In 1998, during the Second World Symposium on Pulmonary Hypertension (PH) held in Evian, France, a clinical classification of PH was proposed. The aim of the... 
FPAH | activin-receptor-like kinase-1 | bone morphogenetic protein receptor type II | BMPR2 | APAH | familial pulmonary arterial hypertension | IPAH | ALK1 | pulmonary arterial hypertension related to risk factors or associated conditions | VENOOCCLUSIVE-DISEASE | CONTROLLED-TRIAL | CARDIAC & CARDIOVASCULAR SYSTEMS | GLYCOGEN-STORAGE-DISEASE | ARTERIAL-HYPERTENSION | GERMLINE MUTATIONS | CAPILLARY HEMANGIOMATOSIS | SICKLE-CELL-DISEASE | CONTINUOUS INTRAVENOUS EPOPROSTENOL | SCLERODERMA SPECTRUM | PROTEIN-RECEPTOR-II | Pulmonary Veno-Occlusive Disease - diagnosis | Genetic Predisposition to Disease | Hypertension, Pulmonary - diagnosis | Hypertension, Pulmonary - classification | Pulmonary Veno-Occlusive Disease - classification | Humans | Risk Factors | Hypertension, Pulmonary - epidemiology | Pulmonary Veno-Occlusive Disease - epidemiology | Drug approval | Pulmonary hypertension | Genetic disorders | Sarcoidosis | Pulmonary arteries | Embolisms | Lung diseases | Cardiovascular disease | Risk factors | Compression therapy | Sleep disorders | Human immunodeficiency virus--HIV | Collagen | Classification | Amphetamines | Clinical medicine | Drug therapy | Veins & arteries
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4. Full Text Classification—Important Step to Improve Management of Patients with an Open Abdomen
by Björck, Martin and Bruhin, Andreas and Cheatham, Michael and Hinck, Daniel and Kaplan, Mark and Manca, Guiseppe and Wild, Thomas and Windsor, Alastair and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Kärlkirurgi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
World Journal of Surgery, ISSN 0364-2313, 6/2009, Volume 33, Issue 6, pp. 1154 - 1157
This short report is a distillation of the proceedings from a consensus group meeting in January 2009. It outlines a proposed classification system for... 
Medicine & Public Health | Cardiac Surgery | Surgery | Abdominal Surgery | Vascular Surgery | Thoracic Surgery | General Surgery | SURGERY | VACUUM PACK | ABDOMINAL COMPARTMENT SYNDROME | ASSISTED WOUND CLOSURE | INTRAABDOMINAL HYPERTENSION | FASCIAL CLOSURE | EXPERTS | INTERNATIONAL-CONFERENCE | Decompression, Surgical - classification | Guidelines as Topic | Surgical Wound Infection - classification | Tissue Adhesions - classification | Humans | Decompression, Surgical - adverse effects | Abdominal Wall - surgery | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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5. Full Text Histopathological Classification of Cross-Sectional Image–Negative Hyperaldosteronism
by Yamazaki, Yuto and Nakamura, Yasuhiro and Omata, Kei and Ise, Kazue and Tezuka, Yuta and Ono, Yoshikiyo and Morimoto, Ryo and Nozawa, Yukinaga and Gomez-Sanchez, Celso E and Tomlins, Scott A and Rainey, William E and Ito, Sadayoshi and Satoh, Fumitoshi and Sasano, Hironobu
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 04/2017, Volume 102, Issue 4, pp. 1182 - 1192
Context: Approximately half of patients with primary aldosteronism (PA) have clinically evident disease according to clinical (hypertension) and/or laboratory... 
DIAGNOSIS | ALDOSTERONE-PRODUCING ADENOMAS | MULTIPLE ADRENOCORTICAL MICRONODULES | MICROADENOMA | CYP11B2 | ENDOCRINOLOGY & METABOLISM | CLINICAL CHARACTERISTICS | MUTATIONS | PREVALENCE | HYPERTENSION | EXPRESSION | Immunohistochemistry | Sodium-Potassium-Exchanging ATPase - genetics | Plasma Membrane Calcium-Transporting ATPases - genetics | Aldosterone - biosynthesis | Humans | Hyperaldosteronism - pathology | Middle Aged | Adrenal Cortex - metabolism | Hyperaldosteronism - genetics | Male | Hyperaldosteronism - metabolism | Adrenal Cortex - pathology | G Protein-Coupled Inwardly-Rectifying Potassium Channels - genetics | Plasma Membrane Calcium-Transporting ATPases - metabolism | Sodium-Potassium-Exchanging ATPase - metabolism | Calcium Channels, L-Type - genetics | G Protein-Coupled Inwardly-Rectifying Potassium Channels - metabolism | Adult | Female | Aged | High-Throughput Nucleotide Sequencing | Calcium Channels, L-Type - metabolism | Mutation | Hypertension | Evaluation | Hyperplasia | Cortex | Aldosterone synthase | Aldosterone | Gene expression | Nodules | Renin | Histopathology | Classification | Production capacity | Cross sections | Image classification
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6. Full Text EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria
by Ozen, Seza and Pistorio, Angela and Iusan, Silvia M and Bakkaloglu, Aysin and Herlin, Troels and Brik, Riva and Buoncompagni, Antonella and Lazar, Calin and Bilge, Ilmay and Uziel, Yosef and Rigante, Donato and Cantarini, Luca and Hilario, Maria Odete and Silva, Clovis A and Alegria, Mauricio and Norambuena, Ximena and Belot, Alexandre and Berkun, Yackov and Estrella, Amparo Ibanez and Olivieri, Alma Nunzia and Alpigiani, Maria Giannina and Rumba, Ingrida and Sztajnbok, Flavio and Tambic-Bukovac, Lana and Breda, Luciana and Al-Mayouf, Sulaiman and Mihaylova, Dimitrina and Chasnyk, Vyacheslav and Sengler, Claudia and Klein-Gitelman, Maria and Djeddi, Djamal and Nuno, Laura and Pruunsild, Chris and Brunner, Jurgen and Kondi, Anuela and Pagava, Karaman and Pederzoli, Silvia and Martini, Alberto and Ruperto, Nicolino and PRINTO and Paediatric Rheumatology International Trials Organisation (PRINTO) and for the Paediatric Rheumatology International Trials Organisation (PRINTO)
Annals of the Rheumatic Diseases, ISSN 0003-4967, 05/2010, Volume 69, Issue 5, pp. 798 - 806
Objectives To validate the previously proposed classification criteria for Henoch–Schönlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener... 
RHEUMATOLOGY 1990 CRITERIA | RHEUMATOLOGY | Granulomatosis with Polyangiitis - diagnosis | Polyarteritis Nodosa - diagnosis | Takayasu Arteritis - diagnosis | Humans | Terminology as Topic | International Cooperation | Purpura, Schoenlein-Henoch - diagnosis | Purpura, Schoenlein-Henoch - classification | Takayasu Arteritis - classification | Epidemiologic Methods | Adolescent | Granulomatosis with Polyangiitis - classification | Polyarteritis Nodosa - classification | Child | Demographic aspects | Takayasu's arteritis | Diagnosis | Research | Periarteritis nodosa | Schonlein-Henoch purpura | Identification and classification | Wegener's granulomatosis | Hypertension | Disease | Physicians | Biopsy | Laboratories | Coronary vessels | Classification | Rheumatology | Data collection | Agreements | Age
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7. Full Text Hypertensive Disorders of Pregnancy: ISSHP Classification, Diagnosis, and Management Recommendations for International Practice
by Brown, Mark A and Magee, Laura A and Kenny, Louise C and Karumanchi, S Ananth and McCarthy, Fergus P and Saito, Shigeru and Hall, David R and Warren, Charlotte E and Adoyi, Gloria and Ishaku, Salisu and Int Soc Study Hypertension Pregnan and International Society for the Study of Hypertension in Pregnancy (ISSHP)
Hypertension, ISSN 0194-911X, 07/2018, Volume 72, Issue 1, pp. 24 - 43
CREATININE RATIO | CARDIOVASCULAR-DISEASE RISK | GESTATIONAL HYPERTENSION | SPOT URINARY PROTEIN | PERIPHERAL VASCULAR DISEASE | SUSPECTED PREECLAMPSIA | INTRAUTERINE GROWTH RESTRICTION | POSTPARTUM HYPERTENSION | ONSET PREECLAMPSIA | URIC-ACID | ANGIOGENIC FACTORS
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8. Full Text Diagnosis: From classification to prediction
by Armstrong, David
Social Science & Medicine, ISSN 0277-9536, 09/2019, Volume 237, p. 112444
Over the last two decades diagnostic labels have increasingly been sub-divided based on molecular and genetic ‘signatures’. But this emphasis on disease... 
Prognosis | Diagnosis | Classification | Prediction | MORTALITY | DEFINITION | SOCIAL SCIENCES, BIOMEDICAL | RISK | PATHOLOGY | BREAST-CANCER | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | BORDERLINE HYPERTENSION | CORONARY-HEART-DISEASE | SEVERITY | SOCIOLOGY
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9. Haemodynamic definitions and updated clinical classification of pulmonary hypertension
by Simonneau, Gérald and Montani, David and Celermajer, David S and Denton, Christopher P and Gatzoulis, Michael A and Krowka, Michael and Williams, Paul G and Souza, Rogerio
The European respiratory journal, ISSN 0903-1936, 01/2019, Volume 53, Issue 1
Since the 1st World Symposium on Pulmonary Hypertension (WSPH) in 1973, pulmonary hypertension (PH) has been arbitrarily defined as mean pulmonary arterial... 
RHEUMATOID-ARTHRITIS | PRESSURE | LONG-TERM RESPONSE | RISK-FACTOR | VENOOCCLUSIVE DISEASE | RESPIRATORY SYSTEM | ARTERIAL-HYPERTENSION | SICKLE-CELL-DISEASE | RIGHT HEART CATHETERIZATION | CALCIUM-CHANNEL BLOCKERS | HEPATITIS-C
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10. Full Text SMASH-U: A proposal for etiologic classification of intracerebral hemorrhage
by Meretoja, Atte and Strbian, Daniel and Putaala, Jukka and Curtze, Sami and Haapaniemi, Elena and Mustanoja, Satu and Sairanen, Tiina and Satopää, Jarno and Silvennoinen, Heli and Niemelä, Mika and Kaste, Markku and Tatlisumak, Turgut
Stroke, ISSN 0039-2499, 10/2012, Volume 43, Issue 10, pp. 2592 - 2597
Background and Purpose-The purpose of this study was to provide a simple and practical clinical classification for the etiology of intracerebral hemorrhage... 
amyloid angiopathy | hypertension | stroke | anticoagulation | etiology | ICH | SUBTYPE | REGISTER | CEREBRAL AMYLOID ANGIOPATHY | FINLAND | LOBAR | VALIDATION | CLINICAL NEUROLOGY | HOSPITAL DISCHARGE | THROMBOLYSIS | PERIPHERAL VASCULAR DISEASE | PERFECT STROKE | WARFARIN USE | Reproducibility of Results | Prognosis | Vascular Diseases - complications | Humans | Middle Aged | Cerebral Hemorrhage - mortality | Male | Survival Rate | Cerebral Amyloid Angiopathy - complications | Aged, 80 and over | Hypertension - complications | Adult | Cerebral Hemorrhage - classification | Classification - methods | Female | Aged | Retrospective Studies | Cerebral Hemorrhage - etiology
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