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Klinefelter Syndrome

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161. Dermatoglyphics in XXYY Klinefelter's syndrome. Full Text available with Trip Pro

Dermatoglyphics in XXYY Klinefelter's syndrome. 5927873 1967 02 24 2018 11 13 0002-9297 18 6 1966 Nov American journal of human genetics Am. J. Hum. Genet. Dermatoglyphics in XXYY Klinefelter's syndrome. 507-13 Alter M M Gorlin R R Yunis J J Peagler F F Bruhl H H eng Journal Article United States Am J Hum Genet 0370475 0002-9297 AIM IM Dermatoglyphics Female Humans Karyotyping Klinefelter Syndrome Leukocytes Male 1966 11 1 1966 11 1 0 1 1966 11 1 0 0 ppublish 5927873 PMC1706194 Chromosoma

1966 American Journal of Human Genetics

162. Klinefelter's syndrome associated with peroneal muscular atrophy. Full Text available with Trip Pro

Klinefelter's syndrome associated with peroneal muscular atrophy. 5636295 1968 03 30 2018 11 13 0035-9157 61 1 1968 Jan Proceedings of the Royal Society of Medicine Proc. R. Soc. Med. Klinefelter's syndrome associated with peroneal muscular atrophy. 86 Jenkins C O CO Ferriman D D eng Case Reports Journal Article England Proc R Soc Med 7505890 0035-9157 IM Adult Gynecomastia Humans Klinefelter Syndrome complications Male Muscular Atrophy complications Obesity complications Sex Chromatin 1968 1 1

1968 Proceedings of the Royal Society of Medicine

163. Klinefelter's Syndrome due to XXYY Chromosome Anomaly Full Text available with Trip Pro

Klinefelter's Syndrome due to XXYY Chromosome Anomaly 14118704 1996 12 01 2018 12 01 0008-4409 90 1964 Feb 29 Canadian Medical Association journal Can Med Assoc J KLINEFELTER'S SYNDROME DUE TO XXYY CHROMOSOME ANOMALY. 590-2 TABATA T T FEDOROFF S S GERRARD J W JW eng Journal Article Canada Can Med Assoc J 0414110 0008-4409 OM Chromosome Aberrations Chromosome Disorders Chromosomes Humans Klinefelter Syndrome CHROMOSOME ABNORMALITIES KLINEFELTER'S SYNDROME 1964 2 29 1964 2 29 0 1 1964 2 29 0 0

1964 Canadian Medical Association Journal

164. The XXYY Variant of Klinefelter's Syndrome Full Text available with Trip Pro

The XXYY Variant of Klinefelter's Syndrome Three males with an XXYY sex chromosome complex are described. These patients, together with five XXYY subjects recorded in the literature, show the clinical features of Klinefelter's syndrome. Taking into consideration the findings in XYY and XXXYY individuals, it appears that the addition of a Y chromosome to XY, XXY and XXXY complexes has a variable and as yet not clearly delineated harmful effect. For example, a 44 + XXYY complement of chromosomes

1964 Canadian Medical Association Journal

165. Klinefelter's Syndrome (XXXXY Variant) Full Text available with Trip Pro

Klinefelter's Syndrome (XXXXY Variant) 14208044 1996 12 01 2018 12 01 0035-9157 57 1964 Sep Proceedings of the Royal Society of Medicine Proc. R. Soc. Med. KLINEFELTER'S SYNDROME (XXXXY VARIANT). 842 COLES H M HM eng Journal Article England Proc R Soc Med 7505890 0035-9157 OM Child Chromosomes Humans Klinefelter Syndrome CHILD CHROMOSOMES KLINEFELTER'S SYNDROME 1964 9 1 1964 9 1 0 1 1964 9 1 0 0 ppublish 14208044 PMC1898724

1964 Proceedings of the Royal Society of Medicine

166. Carcinoma of Male Breast in Association with the Klinefelter Syndrome Full Text available with Trip Pro

Carcinoma of Male Breast in Association with the Klinefelter Syndrome 14228155 1996 12 01 2018 12 01 0007-1447 1 5429 1965 Jan 23 British medical journal Br Med J CARCINOMA OF MALE BREAST IN ASSOCIATION WITH THE KLINEFELTER SYNDROME. 223-5 JACKSON A W AW MULDAL S S OCKEY C H CH O'CONNOR P J PJ eng Journal Article England Br Med J 0372673 0007-1447 0 17-Ketosteroids 0 Adrenal Cortex Hormones 0 Gonadotropins OM 17-Ketosteroids Adenocarcinoma Adenocarcinoma, Scirrhous Adrenal Cortex Hormones (...) Biopsy Breast Breast Neoplasms Carcinoma, Ductal Chromosomes Fluids and Secretions Gonadotropins Gynecomastia Humans Klinefelter Syndrome Male Neoplasm Metastasis Neoplasms diagnosis Pathology Urine 17-KETOSTEROIDS ADENOCARCINOMA ADRENAL CORTEX HORMONES BIOPSY BREAST NEOPLASMS CARCINOMA, DUCTAL CARCINOMA, SCIRRHOUS CHROMOSOMES EXCRETION GONADOTROPINS GYNECOMASTIA KLINEFELTER'S SYNDROME NEOPLASM DIAGNOSIS NEOPLASM METASTASIS PATHOLOGY URINE 1965 1 23 1965 1 23 0 1 1965 1 23 0 0 ppublish 14228155

1965 British medical journal

167. Male Breast Cancer in Klinefelter's Syndrome Full Text available with Trip Pro

Male Breast Cancer in Klinefelter's Syndrome 14238690 1996 12 01 2018 12 01 0007-1447 1 5433 1965 Feb 20 British medical journal Br Med J MALE BREAST CANCER IN KLINEFELTER'S SYNDROME. 521-2 SANDISON A T AT eng Journal Article England Br Med J 0372673 0007-1447 0 Contraceptive Agents, Female 0 Estradiol Congeners 0 Estrogens 731DCA35BT Diethylstilbestrol OM Breast Neoplasms Breast Neoplasms, Male Contraceptive Agents, Female Diethylstilbestrol Estradiol Congeners Estrogens therapeutic use Female (...) Humans Klinefelter Syndrome Male Pathology BREAST NEOPLASMS DIETHYLSTILBESTROL ESTROGENS, THERAPEUTIC KLINEFELTER'S SYNDROME PATHOLOGY 1965 2 20 1965 2 20 0 1 1965 2 20 0 0 ppublish 14238690 PMC2165815 Am J Pathol. 1963 Nov;43:797-807 14075015

1965 British medical journal

168. Coexisting Cretinism and Klinefelter's Syndrome Full Text available with Trip Pro

Coexisting Cretinism and Klinefelter's Syndrome 14273526 1996 12 01 2018 12 01 0007-1447 1 5443 1965 May 01 British medical journal Br Med J COEXISTING CRETINISM AND KLINEFELTER'S SYNDROME. 1170 BOYLE J A JA MCGIRR E M EM eng Journal Article England Br Med J 0372673 0007-1447 OM Congenital Hypothyroidism Diagnosis Humans Klinefelter Syndrome CRETINISM DIAGNOSIS KLINEFELTER'S SYNDROME 1965 5 1 1965 5 1 0 1 1965 5 1 0 0 ppublish 14273526 PMC2166518 J Ment Defic Res. 1960 Dec;4:89-107 13687231 J

1965 British medical journal

169. Klinefelter's syndrome. A report of a case with chromosome analysis. Full Text available with Trip Pro

Klinefelter's syndrome. A report of a case with chromosome analysis. 13982441 1998 11 01 2018 12 01 36 1962 Quarterly bulletin. Northwestern University (Evanston, Ill.). Medical School Q Bull Northwest Univ Med Sch Klinefelter's syndrome. A report of a case with chromosome analysis. 357-62 ROGUSKA J J NADLER C F CF eng Journal Article United States Q Bull Northwest Univ Med Sch 19220080R OM Chromosomes Humans Klinefelter Syndrome CHROMOSOMES KLINEFELTER'S SYNDROME 1962 1 1 1962 1 1 0 1 1962 1 1

1962 Quarterly Bulletin of the Northwestern University Medical School

170. Chromatin-positive Presumed Klinefelter's Syndrome Full Text available with Trip Pro

Chromatin-positive Presumed Klinefelter's Syndrome 13718075 1998 11 01 2018 11 30 0007-1447 1 5226 1961 Mar 04 British medical journal Br Med J Chromatin-positive presumed Klinefelter's syndrome. Survey of boys in London schools for educationally subnormal children. 633-5 ISRAELSOHN W J WJ TAYLOR A I AI eng Journal Article England Br Med J 0372673 0007-1447 0 Chromatin OM Biometry Child Chromatin Chromosome Structures Humans Intellectual Disability complications Klinefelter Syndrome statistics (...) & numerical data London Male Schools KLINEFELTER'S SYNDROME/statistics MENTAL DEFICIENCY/complications 1961 3 4 1961 3 4 0 1 1961 3 4 0 0 ppublish 13718075 PMC1953505 Lancet. 1957 Jul 27;273(6987):164-7 13450359 Lancet. 1958 May 3;1(7027):928-31 13540215 Schweiz Med Wochenschr. 1958 Sep 20;88(38):917-20 13592195 Lancet. 1959 Jan 31;1(7066):217-9 13631971 Nature. 1959 Jan 31;183(4657):302-3 13632697 Nord Med. 1960 Mar 3;63:256-8 13809207 Lancet. 1960 Jul 23;2(7143):184-7 13822249 Lancet. 1959 Aug 22;2(7095

1961 British medical journal

171. A Probable XXYY Sex Determining Mechanism in a Mentally Defective Male with Klinefelter's Syndrome Full Text available with Trip Pro

A Probable XXYY Sex Determining Mechanism in a Mentally Defective Male with Klinefelter's Syndrome 13690987 1998 11 01 2018 11 30 0008-4409 84 1961 Apr 22 Canadian Medical Association journal Can Med Assoc J A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome. 873-8 CARR D H DH BARR M L ML PLUNKETT E R ER eng Case Reports Journal Article Canada Can Med Assoc J 0414110 0008-4409 OM Humans Intellectual Disability Klinefelter Syndrome Male Medical

1961 Canadian Medical Association Journal

172. Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents. Full Text available with Trip Pro

Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents. 5708021 1969 03 20 2018 11 13 0022-2593 5 3 1968 Sep Journal of medical genetics J. Med. Genet. Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents. 161-4 Froland A A Sanger R R Race R R RR eng Journal Article England J Med Genet 2985087R 0022-2593 0 Blood Group Antigens IM Adolescent Adult Aged Blood Group Antigens Child Child, Preschool Female Humans Infant Klinefelter (...) Syndrome blood genetics Male Maternal Age Middle Aged Mosaicism Sex Chromosomes 1968 9 1 1968 9 1 0 1 1968 9 1 0 0 ppublish 5708021 PMC1468647 J Med Genet. 1966 Sep;3(3):162-8 5971052 Lancet. 1958 May 3;1(7027):928-31 13540215 Exp Cell Res. 1960 Sep;20:613-6 13772379 Ann Hum Genet. 1963 Jun;26:297-304 13959333 Lancet. 1963 Nov 23;2(7317):1121-2 14063437 Lancet. 1964 Sep 12;2(7359):589 14172378 Lancet. 1964 May 2;1(7340):955-6 14121353

1968 Journal of Medical Genetics

173. Congenital hypothyroidism in Klinefelter's syndrome. Full Text available with Trip Pro

Congenital hypothyroidism in Klinefelter's syndrome. Congenital hypothyroidism has been found in four patients with Klinefelter's syndrome. It is likely that this reflects more than chance concurrence of these conditions.

1979 Journal of Medical Genetics

174. Interventions Targeting Sensory Challenges in Children with Autism Spectrum Disorder - An Update

and cerebellum of three older men with fragile X syndrome. Mol Autism. 2011;2(1):2. doi: 10.1186/2040-2392-2-2. PMID: 21303513.X-1 653. Greer RD, Pistoljevic N, Cahill C, et al. Effects of conditioning voices as reinforcers for listener responses on rate of learning, awareness, and preferences for listening to stories in preschoolers with autism. Anal Verbal Behav. 2011;27(1):103- 24. PMID: 22532758.X-1, X-3, X-4 D-56 654. Griffith GM, Hastings RP, Oliver C, et al. Psychological well-being in parents (...) of children with Angelman, Cornelia de Lange and Cri du Chat syndromes. J Intellect Disabil Res. 2011 Apr;55(4):397-410. doi: 10.1111/j.1365-2788.2011.01386.x. PMID: 21323782.X-1 655. Grow LL, Carr JE, Kodak TM, et al. A comparison of methods for teaching receptive labeling to children with autism spectrum disorders. J Appl Behav Anal. 2011 Fall;44(3):475-98. doi: 10.1901/jaba.2011.44-475. PMID: 21941380.X-3, X-4 656. Guénolé F, Baleyte J-M. Melatonin for sleep-disturbed children with autism spectrum

2017 Effective Health Care Program (AHRQ)

175. European Society of Endocrinology Clinical practice guidelines for the care of girls and women with Turner syndrome

% 45,X mosaicism (⨁⨁◯◯). R 1.3. We suggest that the new general surveillance management guideline apply to TS patients with any karyotype (⨁⨁◯◯). 1.1.1. Definition Turner syndrome is a chromosomal disorder that affects phenotypic females who have one intact X chromosome and complete or partial absence of the second sex chromosome in association with one or more clinical manifestations ( ). Although the traditional definition of TS implies the presence of physical features such as the characteristic (...) facial appearance, with neck webbing and lymphedema ( , ), we suggest that the clinical manifestations of TS should be broadened to include other features, such as linear growth failure, ovarian insufficiency (pubertal delay), early sensorineural hearing loss, distinctive congenital cardiovascular, skeletal, digital and renal anomalies, a particular neurodevelopmental profile, and a constellation of other disorders that are more common in TS, including hypothyroidism and celiac disease ( , , ). Table

2017 European Society of Endocrinology

176. Klinefelter Fertility Preservation

and to establish factors that can be used to predict which of these patients will have a higher likelihood of success with advanced reproductive technology. The hypothesis is that younger Klinefelter patients will have higher sperm retrieval rates. Condition or disease Intervention/treatment Phase Klinefelter Syndrome Procedure: Testicular Biopsy Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 15 participants Intervention (...) , 2014 Last Verified: May 2014 Keywords provided by Boston Children’s Hospital: Klinefelter Fertility Additional relevant MeSH terms: Layout table for MeSH terms Syndrome Klinefelter Syndrome Disease Pathologic Processes Sex Chromosome Disorders of Sex Development Disorders of Sex Development Urogenital Abnormalities Sex Chromosome Disorders Chromosome Disorders Congenital Abnormalities Genetic Diseases, Inborn Gonadal Disorders Endocrine System Diseases Hypogonadism

2013 Clinical Trials

177. Gender Dysphoria and Gender Change in Disorders of Sex Development/Intersex Conditions: Results From the dsd-LIFE Study. (Abstract)

hyperplasia (n = 221). Data on psychosexual outcome were gathered by medical interviews and questionnaires.Gender change and gender dysphoria.Although gender changes were reported by 5% of participants, only in 1% (3% if those with Klinefelter and Turner syndromes-conditions in which gender issues are not prominent-are excluded) did the gender change take place after puberty and was likely initiated by the patient. 39 participants (4%) reported gender variance: between male and female, a gender other than (...) Gender Dysphoria and Gender Change in Disorders of Sex Development/Intersex Conditions: Results From the dsd-LIFE Study. Information on the psychosexual outcome of individuals with disorders of sex development (DSDs) and intersex conditions is of great importance for sex assignment at birth of newborns with DSD.To assess gender change and gender dysphoria in a large sample of individuals with different DSDs.A cross-sectional study was conducted in 14 European centers with 1,040 participants

2018 Journal Of Sexual Medicine

178. Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosity. (Abstract)

Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosity. A higher frequency of twin births in sibships of Klinefelter syndrome patients and also monozygotic or dizygotic twins, themselves being affected by Klinefelter syndrome have been noted repeatedly. To address this issue, we evaluated type and frequency of twinning among Klinefelter fetuses that we had received for autopsy within a 'Prenatal Diagnosis (...) ' program.We performed fetal autopsies, and genetic analyses on DNA extracted from stained histological slides.Among 41 prenatal diagnoses of a 47, XXY karyotype we observed four twin pairs. One was dizygotic with discordant Klinefelter and Down syndrome. Three twin pairs were monozygotic as concluded from monochorial placentation. In two monozygotic pairs one twin partner was an acardiac monster and in one of these the acardiac twin showed a female gonadal sex and missing Y-chromosomal SRY-sequences

2012 Prenatal diagnosis

179. It's not all about the testes: medical issues in Klinefelter patients. (Abstract)

It's not all about the testes: medical issues in Klinefelter patients. Important medical conditions associated with Klinefelter syndrome (KS) are categorized as: 1) motor, cognitive, and behavioral dysfunction; 2) tumors; 3) vascular disease; and 4) endocrine/metabolic and autoimmune diseases. Earlier diagnosis of KS may lead to earlier intervention with effective treatment.Copyright © 2012 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

2012 Fertility and Sterility

180. A 47,XXq-Y Klinefelter male. Full Text available with Trip Pro

A 47,XXq-Y Klinefelter male. 5149539 1972 08 01 2018 11 13 0022-2593 8 4 1971 Dec Journal of medical genetics J. Med. Genet. A 47,XXq-Y Klinefelter male. 530-2 Chandra H S HS Reddy G N GN Peter J J Venkatachalaiah G G eng Case Reports Journal Article England J Med Genet 2985087R 0022-2593 0 Blood Group Antigens 10028-17-8 Tritium VC2W18DGKR Thymidine IM Adolescent Autoradiography Blood Group Antigens Dermatoglyphics Hair cytology Humans Karyotyping Klinefelter Syndrome pathology Lymphocytes

1971 Journal of Medical Genetics

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