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Year | Number of Results |
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2007 | 1 |
2016 | 1 |
2017 | 3 |
2020 | 1 |
2024 | 0 |
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Page 1
Hair Loss: Common Causes and Treatment.
Am Fam Physician. 2017 Sep 15;96(6):371-378.
Am Fam Physician. 2017.
PMID: 28925637
Free article.
Breaking the cycle of hair breakage: pearls for the management of acquired trichorrhexis nodosa.
Haskin A, Kwatra SG, Aguh C.
Haskin A, et al.
J Dermatolog Treat. 2017 Jun;28(4):322-326. doi: 10.1080/09546634.2016.1246704. Epub 2016 Oct 28.
J Dermatolog Treat. 2017.
PMID: 27718775
Review.
It is especially prevalent in black patients with tightly curled hair types and can present unique diagnostic and therapeutic challenges due to structural differences in these hair types and the combination of various hair care and styling practices that contribute …
It is especially prevalent in black patients with tightly curled hair types and can present unique diagnostic and therapeutic challen …
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Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities.
Rasheed M, Shahzad S, Zaeem A, Afzal I, Gul A, Khalid S.
Rasheed M, et al.
Arch Dermatol Res. 2017 Dec;309(10):773-785. doi: 10.1007/s00403-017-1780-x. Epub 2017 Sep 14.
Arch Dermatol Res. 2017.
PMID: 28913623
Review.
These syndromes mostly prevail in high consanguinity states, with distinctive clinical features. ...Additionally, we aim to update health professionals about the practice of molecular screening in ichthyosis syndromes for appropriate diagnosis and treatment....
These syndromes mostly prevail in high consanguinity states, with distinctive clinical features. ...Additionally, we aim to update he …
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Abnormal Newborn Screening Follow-up for Severe Combined Immunodeficiency in an Amish Cohort with Cartilage-Hair Hypoplasia.
Scott EM, Chandra S, Li J, Robinette ED, Brown MF, Wenger OK.
Scott EM, et al.
J Clin Immunol. 2020 Feb;40(2):321-328. doi: 10.1007/s10875-019-00739-9. Epub 2020 Jan 6.
J Clin Immunol. 2020.
PMID: 31903518
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Prenatal diagnosis of xeroderma pigmentosum and trichothiodystrophy in 76 pregnancies at risk.
Kleijer WJ, van der Sterre ML, Garritsen VH, Raams A, Jaspers NG.
Kleijer WJ, et al.
Prenat Diagn. 2007 Dec;27(12):1133-7. doi: 10.1002/pd.1849.
Prenat Diagn. 2007.
PMID: 17880036
OBJECTIVE: Evaluation of results in a consecutive series of 76 prenatal diagnoses for xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) made since 1977. METHODS: UV-induced DNA repair synthesis was assessed by the autoradiographic measurement of the incorporation of …
OBJECTIVE: Evaluation of results in a consecutive series of 76 prenatal diagnoses for xeroderma pigmentosum (XP) and trichothiodystrophy …
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