Results 81 to 90 of about 2,252,623 (207)
MRI in Congenital Facial Palsy
Magnetic resonance (MR) findings in a 12-month-old boy with congenital unilateral facial palsy and a 9-month-old girl with atypical Moebius syndrome are reported from the National Center of Neurology and Psychiatry, Kodaira, Japan.
J Gordon Millichap
doaj +1 more source
ABSTRACT Background Poland syndrome is a rare congenital condition characterized by unilateral breast deformity. Autologous fat transplantation has emerged as the preferred treatment due to its minimal invasiveness, rapid recovery, absence of rejection reactions, and potential for multiple surgeries to enhance postoperative outcomes.
Na Wang +5 more
wiley +1 more source
The development and assessment of biological treatments for children [PDF]
The development of biological agents with specific immunological targets has revolutionized the treatment of a wide variety of paediatric diseases where traditional immunosuppressive agents have been partly ineffective or intolerable.
Akobeng +118 more
core +1 more source
A rare case of Moebius sequence
We report a case of an 18-year-old male who presented with watering and inability to close the left eye completely since 6 months and inability to move both eyes outward and to close the mouth since childhood.
Abhishek Kulkarni +3 more
doaj +1 more source
El síndrome de Moebius. Revisión de la literatura y presentación de dos casos clínicos [PDF]
El síndrome de Moebius es un trastorno congénito que se caracteriza por una falta de expresión facial y la ausencia de movilidad ocular debido a la afectación unilateral o bilateral de los pares craneales VI y VIl.
Delgado Molina, Esther +3 more
core
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: Experience of the FSHD Italian National Registry [PDF]
OBJECTIVES: Facioscapulohumeral muscular dystrophy type 1 (FSHD1) has been genetically linked to reduced numbers ( 64 8) of D4Z4 repeats at 4q35. Particularly severe FSHD cases, characterised by an infantile onset and presence of additional extra ...
Angelini, Corrado +30 more
core +4 more sources
Changes in the size of the coronoid process, due to hyperplasia or hypoplasia, may interfere with the normal range of mouth opening. Coronoid hyperplasia is a rare oral and maxillofacial disease which might result in progressive limitation of mouth opening due to the impingement of an abnormal elongated mandibular coronoid process on the zygomatic arch.
Areeg Elmusrati +2 more
wiley +1 more source
The Effect of Small Molecules on Sterol Homeostasis: Measuring 7-Dehydrocholesterol in Dhcr7-Deficient Neuro2a Cells and Human Fibroblasts [PDF]
K
Balogh, István +8 more
core +1 more source
Abstract The newly proposed revised criteria for diagnosis and staging of Alzheimer's disease (AD) by the Alzheimer's Association (AA) Workgroup represent a significant milestone in the field. These criteria offer objective measures for diagnosing and staging biological AD, bridging the gap between research and clinical care.
Clifford R. Jack +13 more
wiley +1 more source
Enactivism, other minds, and mental disorders [PDF]
Although enactive approaches to cognition vary in terms of their character and scope, all endorse several core claims. The first is that cognition is tied to action.
Krueger, Joel
core +2 more sources

