Results 11 to 20 of about 2,842 (59)

O'simliklarda xlorofill pigmenti ahamiyati

open access: yes, 2022
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
core   +1 more source

Queratoacantomas, ¿una manifestación tardía de incontinencia pigmenti? [PDF]

open access: yes, 2019
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
core  

Incontinentia pigmenti in a newborn boy

open access: yes, 2021
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
core   +1 more source

The Impact of Chronic Liver Diseases on the Level of Heart-Type Fatty Acid-Binding Protein (H-FABP) Concentrations [PDF]

open access: yes, 2009
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
core  

Incontinencia pigmenti en un niño [PDF]

open access: yes, 2003
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
core  

Incontinencia pigmenti en estadio vésico ampolloso. Reporte de dos casos [PDF]

open access: yes, 2006
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
core  

Incontinentia Pigmenti [PDF]

open access: yes, 2017
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
core  

Incontinentia pigmenti in a child with suspected retinoblastoma [PDF]

open access: yes, 2017
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
core   +2 more sources

Incontinentia Pigmenti

open access: yes, 2019
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
core   +1 more source

Incontinentia Pigmenti

open access: yes, 2009
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
core   +1 more source

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