Database : MEDLINE
Search on : Chilblains [Words]
References found : 309 [refine]
Displaying: 1 .. 10   in format [Detailed]

page 1 of 31 go to page                         

  1 / 309 MEDLINE  
              next record last record
select
to print
Photocopy

[PMID]: 29402117
[Au] Autor:Bragazzi NL; Raffi A; Siri A; Tornali C; Martini M
[Ti] Title:La medicina del rinascimento e la scoperta della circolazione minore: il ruolo di Michele Serveto (1511­1553). [Renaissance medicine and the discovery of the lesser circulation: the role of Michael Servetus (1511-1553)].
[So] Source:Acta Med Hist Adriat;15(2):271-282, 2017 Dec.
[Is] ISSN:1334-4366
[Cp] Country of publication:Croatia
[La] Language:ita
[Ab] Abstract:Human urine is currently the subject of biomedical investigations as a potential therapeutic resource and it continues to be used in remedies in different cultures and societies, including the Spanish culture. In this study we gather etnomedical knowledge about urotherapy and determine their associated symbolisms in Spain. A literature overview and a case study were carried out to compile urine-based remedies and as a direct analysis of symbolic systems. Urotherapy is widespread in Spanish folk medicine. Among the 204 collected remedies, those related to treatment of diseases or skin conditions predominate (63%). Remedies have been reported for the treatment of skin diseases such as eczema, chloasma, alopecia, etc. to treat or alleviate burns, chilblains, wounds or skin chapping, and as a treatment of venomous bites. Most of the collected remedies have an associated naturalist symbolism, based on local traditions and the transmission of empirical initial knowledge. The use of urine in Spain is a result of the interaction of two types of practice: a local and traditional urotherapy, rural and with a utilitarian purpose, and a technical urotherapy, limited to an urban environment and a naturopathic medicine.
[Pt] Publication type:ENGLISH ABSTRACT; JOURNAL ARTICLE; REVIEW
[Em] Entry month:1802
[Cu] Class update date: 180206
[Lr] Last revision date:180206
[St] Status:In-Data-Review

  2 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 29231259
[Au] Autor:Park KK; Tayebi B; Uihlein L; Speiser J; Mir A; Gerami P; Mancini A; Kim W
[Ad] Address:Dermatology and Plastic Surgery Associates, Joliet, IL, USA.
[Ti] Title:Pernio as the presenting sign of blast crisis in acute lymphoblastic leukemia.
[So] Source:Pediatr Dermatol;35(1):e74-e75, 2018 Jan.
[Is] ISSN:1525-1470
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:A previously healthy 5-year-old girl presented with acute onset of blue toes and red spots on the nose and fingers. The striking nature of these lesions, along with the finding of submandibular lymphadenopathy, prompted further evaluation. Laboratory findings were remarkable for anemia, high transaminase levels, and high blast count. Histopathologic findings were consistent with early pernio. Further examination revealed acute B-cell lymphoblastic leukemia. Treatment of the leukemia led to resolution of the pernio.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 180122
[Lr] Last revision date:180122
[St] Status:In-Process
[do] DOI:10.1111/pde.13366

  3 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 29318596
[Au] Autor:Nazzaro G; Genovese G; Marzano AV
[Ad] Address:Dipartimento di Fisiopatologia e dei Trapianti, University of Milan - Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
[Ti] Title:Idiopathic chilblains in myelomonocytic leukemia: not a simple association.
[So] Source:Int J Dermatol;, 2018 Jan 10.
[Is] ISSN:1365-4632
[Cp] Country of publication:England
[La] Language:eng
[Pt] Publication type:CASE REPORTS
[Em] Entry month:1801
[Cu] Class update date: 180110
[Lr] Last revision date:180110
[St] Status:Publisher
[do] DOI:10.1111/ijd.13896

  4 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 29277929
[Au] Autor:Mohandas P; Bowker R; Ravenscroft J; Bleiker T
[Ad] Address:Department of Dermatology, Royal Derby Hospital, Derby, UK.
[Ti] Title:Recurrent chilblains in a child with neurological impairment.
[So] Source:Clin Exp Dermatol;, 2017 Dec 26.
[Is] ISSN:1365-2230
[Cp] Country of publication:England
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171226
[Lr] Last revision date:171226
[St] Status:Publisher
[do] DOI:10.1111/ced.13330

  5 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28919362
[Au] Autor:Kisla Ekinci RM; Balci S; Bisgin A; Altintas DU; Yilmaz M
[Ad] Address:Department of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, Turkey. Electronic address: mir_kisla@hotmail.com.
[Ti] Title:A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.
[So] Source:Eur J Med Genet;60(12):690-694, 2017 Dec.
[Is] ISSN:1878-0849
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Three prime repair exonuclease 1 degrades single and double stranded DNA with 3'-5' nuclease activity and its mutations are related to type 1 IFN mediated autoinflammation due to accumulated intracellular nucleic acids. To date, several cases of systemic lupus erythematosus, Aicardi-Goutieres syndrome, familial chilblain lupus, retinal vasculopathy-cerebral leukodystrophy have been reported with TREX1 mutations. Chilblain lupus is a skin disease characterized by blue-reddish coloring, swelling or ulcers on acral regions of body such as fingertips, heels, nose and auricles. Central nervous system vasculitis is a prominent cause of childhood strokes. 10 families with familial chilblain lupus related to TREX1 mutations were reported previously in the literature, in which homozygote D18N variant in TREX1 gene was related to chilblains with cerebral vasculitis. In this report, whole-exome-sequencing revealed a homozygote R114C mutation in TREX1 gene was shown in two siblings with recurrent chilblains whom one of them was the second case accompanied by cerebral vasculitis in the literature. As a result, the approach of WES in clinical use revealed a novel mutation in clinically heterogenous patients to provide genetic counseling.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1709
[Cu] Class update date: 171120
[Lr] Last revision date:171120
[St] Status:In-Process

  6 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28913687
[Au] Autor:Joseph L; Kim ESH
[Ad] Address:Division of Cardiovascular Diseases, Department of Internal Medicine, University of Iowa, 169 Newton Road, Iowa City, IA, 52246, USA.
[Ti] Title:Non-Atherosclerotic Vascular Disease in Women.
[So] Source:Curr Treat Options Cardiovasc Med;19(10):78, 2017 Sep 14.
[Is] ISSN:1092-8464
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:OPINION STATEMENT: Takayasu arteritis, fibromuscular dysplasia (FMD), spontaneous arterial dissection, Raynaud's phenomenon, and chilblains are vascular conditions that are associated with an increased predisposition in women and are often underdiagnosed. Takayasu arteritis has an incidence rate of 2.6 cases per million individuals per year in the USA and predominantly affects women of childbearing age. HLA-B5 genetic locus is linked with Takayasu arteritis susceptibility. Methods to determine active disease are limiting; currently utilized clinical and imaging findings and laboratory tests are of limited value for this purpose. Pregnancy poses risks for maternal and fetal complications, and these patients need additional monitoring and care before and after conception. Controlling hypertension and immunosuppression using steroids, biological and non-biological immunosuppressants, are key components of managing patients with this arteritis. FMD commonly affects middle-aged, white females. Its true prevalence is unknown. Renal and cerebrovascular beds are the most frequently involved vascular beds. Its clinical presentation varies from no symptoms to catastrophic events. Controlling vascular risk factors, periodic surveillance, and revascularization when indicated are important factors in FMD management. Spontaneous arterial dissections are less common, but are an important cause of morbidity and mortality in specific populations. Cervicocephalic dissection causes 10-20% of the strokes in young adults, and coronary artery dissection is the culprit in almost one fourth of young women presenting with acute myocardial infarction. Early diagnosis is key to improving prognosis in these patients, as the majority of patients have spontaneous resolution of the dissection with conservative management alone. Increased clinician awareness of the presentation features and angiographic findings are imperative for early diagnosis. Raynaud's phenomenon and chilblains are cold- or stress-induced cutaneous lesions, commonly involving distal extremities. Secondary causes such as connective tissue diseases and malignancies must be thoroughly excluded during evaluation of these conditions. Cold avoidance, systemic and local warming, and oral vasodilator therapy are the mainstays of therapy.
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Em] Entry month:1709
[Cu] Class update date: 170919
[Lr] Last revision date:170919
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.1007/s11936-017-0579-6

  7 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28770006
[Au] Autor:Otter SJ; Rohan M; Davies KA; Kumar S; Gow P; Dalbeth N; Corkill M; Panthakalam S; Rome K
[Ad] Address:Health and Research Rehabilitation Institute and School of Podiatry, AUT University, Auckland, New Zealand.
[Ti] Title:Categorisation of foot complaints in systemic lupus erythematosus (SLE) from a New Zealand cohort.
[So] Source:J Foot Ankle Res;10:33, 2017.
[Is] ISSN:1757-1146
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:BACKGROUND: Foot complaints have been shown to be common in systemic lupus erythematosus (SLE) and heterogeneous in nature. We aimed to categorize self-reported foot complaints in people with SLE and foot symptoms. METHODS: A self-administered validated questionnaire was posted to 406 people with SLE attending adult rheumatology clinics across three health boards in Auckland, New Zealand. In addition to foot pain, vascular complaints, dermatological lesions and neurological symptoms were included in the analysis. Pairwise correlations among the variables were undertaken followed by factor analysis to identify and categorise associations between reported foot complaints. RESULTS: From the questionnaires returned, 93 full datasets were analysed. Participants' were predominantly female ( = 87, 93.7%), with mean (SD) age of 50.4 (14.3) years and a mean (SD) disease duration of 13.1 (11) years. Three categories of foot complaint were determined: 'foot pain', 'skin disorders' and 'vascular insufficiency'. These three groups provided the best fit (0.91) to describe the wide range of foot complaints reported by those with SLE. Factor analysis for foot pain demonstrated a high positive loading for the inter-correlation of foot pain in past month (0.83), foot pain today (0.71), intermittent claudication (0.71), numbness (0.62), loss of balance (0.81), swelling (0.59), foot joint pain (0.77), arch pain (0.68) and tendon pain (0.77). Skin disorders demonstrated a very high positive loading for 3 factors skin rash (0.82), blistering skin rash (0.95) and foot ulceration (0.88). In vascular insufficiency a high positive loading for cold feet (0.83), chilblains (0.76) and Raynaud's phenomenon (0.70). CONCLUSIONS: This work suggests people with SLE report three independent categories of foot complaints; foot pain, skin disorders or vascular insufficiency.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1708
[Cu] Class update date: 170807
[Lr] Last revision date:170807
[St] Status:In-Process
[do] DOI:10.1186/s13047-017-0217-2

  8 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy

[PMID]: 28767264
[Au] Autor:Vallejo JR; Aparicio Mena AJ; González JA
[Ad] Address:Departamento de Terapéutica Médico-Quirúrgica, Facultad de Medicina, Universidad de Extremadura, Badajoz, Spain. joseramonvallejo@unex.es.
[Ti] Title:Human urine-based therapeutics in Spain from the early 20th century to the present: a historical literature overview and a present-day case study.
[So] Source:Acta Med Hist Adriat;15(1):73-108, 2017 Jun.
[Is] ISSN:1334-4366
[Cp] Country of publication:Croatia
[La] Language:eng
[Ab] Abstract:Human urine is currently the subject of biomedical investigations as a potential therapeutic resource and it continues to be used in remedies in different cultures and societies, including the Spanish culture. In this study we gather etnomedical knowledge about urotherapy and determine their associated symbolisms in Spain. A literature overview and a case study were carried out to compile urine-based remedies and as a direct analysis of symbolic systems. Urotherapy is widespread in Spanish folk medicine. Among the 204 collected remedies, those related to treatment of diseases or skin conditions predominate (63%). Remedies have been reported for the treatment of skin diseases such as eczema, chloasma, alopecia, etc. to treat or alleviate burns, chilblains, wounds or skin chapping, and as a treatment of venomous bites. Most of the collected remedies have an associated naturalist symbolism, based on local traditions and the transmission of empirical initial knowledge. The use of urine in Spain is a result of the interaction of two types of practice: a local and traditional urotherapy, rural and with a utilitarian purpose, and a technical urotherapy, limited to an urban environment and a naturopathic medicine.
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Em] Entry month:1708
[Cu] Class update date: 171117
[Lr] Last revision date:171117
[St] Status:In-Process

  9 / 309 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28332073
[Au] Autor:Abdel-Salam GMH; Abdel-Hamid MS; Mohammad SA; Abdel-Ghafar SF; Soliman DR; El-Bassyouni HT; Effat L; Zaki MS
[Ad] Address:Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt. ghada.abdelsalam@yahoo.com.
[Ti] Title:Aicardi-Goutières syndrome: unusual neuro-radiological manifestations.
[So] Source:Metab Brain Dis;32(3):679-683, 2017 Jun.
[Is] ISSN:1573-7365
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Aicardi-Goutières syndrome (AGS) is one of the expanding group of inherited congenital infection like syndromes. Here, we describe the detailed clinical and imaging findings of two sibs with AGS. Each shows scattered periventricular intracranial calcifications, severe global delay, seizures, microcephaly and spasticity. Interestingly, chilblains were observed in the two sisters as well as their parents and a paternal uncle. The brain MRI of the older sister showed marked ventricular dilatation as a result of unusual associated porencephalic cysts. Unexpectedly, unilateral cerebellar hypoplasia was also noted. In comparison, her younger sister displayed the classic atrophic changes and white matter loss of AGS. The diagnosis of AGS was confirmed by sequence analysis, which identified a previously reported homozygous RNASEH2B mutation, c.554 T > G (p.V185G). Parents were heterozygous for the same mutation. Further molecular analysis excluded mutations in potentially related manifestations of COL4A1 gene. This is the first report of chilblains associated with heterozygous RNASEH2B mutation. Further, the brain imaging findings appear particularly interesting, which until now has not been reported in any AGS patient. We discuss the possible reasons for this unusual presentation.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1703
[Cu] Class update date: 171030
[Lr] Last revision date:171030
[St] Status:In-Process
[do] DOI:10.1007/s11011-017-9993-4

  10 / 309 MEDLINE  
              first record previous record
select
to print
Photocopy
Full text

[PMID]: 28216727
[Au] Autor:Singh LC
[Ad] Address:Department of Dermatology, Military Hospital, Ahmedabad, Gujarat, India.
[Ti] Title:High Altitude Dermatology.
[So] Source:Indian J Dermatol;62(1):59-65, 2017 Jan-Feb.
[Is] ISSN:1998-3611
[Cp] Country of publication:India
[La] Language:eng
[Ab] Abstract:Approximately, 140 million people worldwide live permanently at high altitudes (HAs) and approximately another 40 million people travel to HA area (HAA) every year for reasons of occupation, sports or recreation. In India, whole of Ladakh region, part of Northwest Kashmir, Northern part of Sikkim and Tenga valley of Arunachal are considered inhabited areas of HAA. The low quantity of oxygen, high exposure of ultraviolet (UV) light, very low humidity, extreme subzero temperature in winter, high wind velocity, make this region difficult for lowlanders as well as for tourists. Acute mountain sickness, HA pulmonary edema, HA cerebral edema, and thromboembolic conditions are known to occur in HA. However, enough knowledge has not been shared on dermatoses peculiar to this region. Xerosis, UV-related skin disorders (tanning, photomelanosis, acute and chronic sunburn, polymorphic light eruption, chronic actinic dermatitis, actinic cheilitis, etc.), cold injuries (frostbite, chilblains, acrocyanosis, erythrocyanosis, etc.) nail changes (koilonychias), airborne contact dermatitis, insect bite reaction, and skin carcinoma (basal cell carcinomas, squamous cell carcinomas, and also rarely malignant melanoma) are the dermatoses seen in HAAs. Early diagnosis and knowledge of HA dermatoses may prevent serious consequences of disease and improve the quality of life for the visitors as well as for native of the place.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1702
[Cu] Class update date: 170223
[Lr] Last revision date:170223
[St] Status:In-Data-Review
[do] DOI:10.4103/0019-5154.198050


page 1 of 31 go to page                         
   


Refine the search
  Database : MEDLINE Advanced form   

    Search in field  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information