Results 1 to 10 of about 1,177,850 (201)

Congenital Abnormalities and Multiple Sclerosis [PDF]

open access: yesBMC Neurology, 2010
Background There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased ...
Orton Sarah-Michelle   +7 more
doaj   +4 more sources

Chromosome 1q21 abnormalities in multiple myeloma [PDF]

open access: yesBlood Cancer Journal, 2021
Gain of chromosome 1q (+1q) is one of the most common recurrent cytogenetic abnormalities in multiple myeloma (MM), occurring in approximately 40% of newly diagnosed cases.
Timothy M. Schmidt   +2 more
doaj   +3 more sources

Multiple Congenital Heart Abnormalities [PDF]

open access: yesActa Medica Bulgarica, 2019
Congenital heart abnormalities are rare and most often occur separately. These structural and functional disorders can cause a range of diseases that vary in severity, from mild or even asymptomatic to severe and life-threatening.
Lazarov S., Bogdanov G., Nikolov R.
doaj   +2 more sources

Systemic multiple myeloma and colonic abnormalities

open access: yesVideoGIE, 2023
Video 1Colonic abnormalities observed in the course of systemic multiple myeloma.
Katarzyna M. Pawlak, MD, PhD, MRCPUK   +3 more
doaj   +3 more sources

NF1 with Multiple Cardiac Structural Abnormalities Leading to Cerebral Infarction [PDF]

open access: yesDiagnostics
Background/Objectives: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder driven by mutations in the NF1 gene, whose pathogenesis centers on the loss of neurofibromin function and subsequent hyperactivation of the RAS/MAPK pathway. Notably,
Jingwei Ye   +3 more
doaj   +2 more sources

Arthrogryposis: A Rare Manifestation in Infant of Diabetic Mother [PDF]

open access: yesOnline Journal of Health & Allied Sciences, 2009
Arthrogryposis multiplex congenita is characterized by non-progressive, multiple joint contractures present at birth. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities like neurogenic, muscle, connective tissue abnormalities ...
Amar M. Taksande   +2 more
doaj   +1 more source

Anatomical mapping of vascular anomalies of the lips [PDF]

open access: yesRevista Brasileira de Cirurgia Plástica, 2020
Introduction: The lip is the body region more often affected by vascular anomalies (VAs). Identifying the appropriate etiology of the lesion is significantly important when determining the treatment of choice for the patient.
Rafael Ferreira Zatz   +4 more
doaj   +1 more source

Anatomic and histological characteristics of vagina reconstructed by McIndoe method [PDF]

open access: yesVojnosanitetski Pregled, 2009
Background/Aim. Congenital absence of vagina is known from ancient times of Greek. According to the literature data, incidence is 1/4 000 to 1/20 000. Treatment of this anomaly includes non-operative and operative procedures. McIndoe procedure uses split
Kozarski Jefta   +2 more
doaj   +1 more source

Periventricular magnetisation transfer abnormalities in early multiple sclerosis

open access: yesNeuroImage: Clinical, 2022
Objective: Recent studies suggested that CSF-mediated factors contribute to periventricular (PV) T2-hyperintense lesion formation in multiple sclerosis (MS) and this in turn correlates with cortical damage.
Lukas Pirpamer   +9 more
doaj   +1 more source

Multiple corticosteroid abnormalities in cats with hyperaldosteronism

open access: yesJournal of Veterinary Internal Medicine, 2021
Background The frequency with which multiple corticosteroid abnormalities occur in cats with aldosterone secreting adrenocortical tumors is unknown. Objectives To evaluate adrenal‐derived corticosteroids in cats in which blood samples were submitted for ...
Daniel K. Langlois   +3 more
doaj   +1 more source

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