Results 11 to 20 of about 2,842 (59)
O'simliklarda xlorofill pigmenti ahamiyati
Xlorofill pigmenti òsimliklar uchun ahamiyati, kimyoviy xossalari haqida ba'zi ...
Jovliyev Baxtiyor Xolboyevich1, Javliyev Furqat Baxtiyorovich2, Qo'yliyeva Mahbuba Uzoqovna2, Ulug'murodov Temurbek3, Kulberdiyev Abdullo3, Shodiyev Abdulaziz3
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Queratoacantomas, ¿una manifestación tardía de incontinencia pigmenti? [PDF]
We report a female patient with stage 3 Incontinentia Pigmenti (IP), linear pigmented patches following Blaschko’s lines which involve both torso and extremities.
Rueda, Ricardo +2 more
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Incontinentia pigmenti in a newborn boy
Incontinentia pigmenti is an uncommon X-linked dominant neurocutaneous ectodermal dysplasia. The disorder is usually lethal in males in utero, although it may occasionally occur in males with somatic mosaicsism or Klinefelter syndrome.
Bergmann, Kristin +4 more
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The Impact of Chronic Liver Diseases on the Level of Heart-Type Fatty Acid-Binding Protein (H-FABP) Concentrations [PDF]
Heart-type fatty acid binding-protein (H-FABP) has been reported to be a potential novel biochemical marker for the early diagnosis of acute myocardial infarction (AMI). The presence of H-FABP in the liver has not been reported. The aim of this study was
William, Brent +2 more
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Incontinencia pigmenti en un niño [PDF]
La incontinencia pigmenti (IP) es una enfermedad infrecuente, con un patrón de herencia dominante ligado al cromosoma X, caracterizada por anormalidades del tejido ectodérmico.
Soto Abi-Saab, Clara +1 more
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Incontinencia pigmenti en estadio vésico ampolloso. Reporte de dos casos [PDF]
La incontinencia pigmenti es una genodermatosis multisistémica ligada al cromosoma X, caracterizada por lesiones cutáneas que evolucionan a través de cuatro estadios.
Toro Giraldo, Ana Milena +3 more
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A case of incontinentia pigmenti in a 1-month-old infant girl is described. The patient had an associated raised alkaline phosphatase level, hyperphosphataemia, as well as abnormalities of the plasma proteins.
Perlman, MM
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Incontinentia pigmenti in a child with suspected retinoblastoma [PDF]
Background Incontinentia pigmenti is a rare X-linked dominant syndrome caused by mutation in the NEMO/IKKgamma gene, and characterized by a spectrum of cutaneous, ocular, neurologic and dental abnormalities.
Archana Srinivasan +7 more
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Incontinentia pigment! (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysptasia. It is an X-linked dominant disorder caused by mutations in the IKBKG/NEMO gene on Xq28. Approximately 80% of patients have a deletion of exons 4 to 10.
CammarataScalisi F, Fusco F, Ursini M V
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L'incontinentia pigmenti è una sindrome ereditaria X-linked, letale nel maschio, che presenta manifestazioni cutanee polimorfe, differenti a seconda delle diverse epoche della ...
NERI, IRIA +2 more
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