Results 51 to 60 of about 4,848 (107)

The Obstructive Sleep Apnea Physical Exam: A Systematic Review and Meta-Analysis. [PDF]

Laryngoscope Investig Otolaryngol
Punjabi N, Qu RW, Vacaru A, Pandey B, Tamares S, Inman JC.   +5 more
europepmc   +1 more source

A Rare Compound Heterozygous NAGLU Gene Mutation in Two Siblings with Mucopolysaccharidosis type Iiib. [PDF]

Iran J Pathol
Vahedi-Larijani L, Sotoudeh Anvari M, Biglari A, Nabati M, Banihashemi H, Mohammadi Kharkeshi M.   +5 more
europepmc   +1 more source

Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region. [PDF]

Clin Epigenetics
Urakawa T, Kanamaru Y, Amano N, Uchida A, Fukami M, Kagami M.   +5 more
europepmc   +1 more source

Light Chain (AL) Amyloidosis Masquerading as Scleroderma: A Diagnostic Challenge. [PDF]

J Hematol
Dhamija K, Jiwani RA, Lakshaman A, Sadashiv S, Mewawalla P.   +4 more
europepmc   +1 more source

Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management. [PDF]

J Clin Med
Comisi FF, Esposito E, Savasta S.
europepmc   +1 more source

Macroglossia.

Indian pediatrics, 2004
A K, Dubey, Kirandeep, Sodhi
openaire   +1 more source

Phenotypes of headache in patients with obstructive sleep apnea. [PDF]

Sci Rep
Tripakornkusol V, Sinsopa N, Khamsai S, Sawanyawisuth K.   +3 more
europepmc   +1 more source

Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature.

J Indian Assoc Pediatr Surg
Achugatla S, Singh S, Thakur S, Redkar R.   +3 more
europepmc   +1 more source

The Successful Anesthetic Management of an Adult With Cri-du-Chat Syndrome by Using Personalized Behavioral Strategies: A Case Report. [PDF]

Cureus
Mavridou P, Exarchos C, Kitsakou P, Panagiotou P.   +3 more
europepmc   +1 more source

Case Report: Novel mutations in two patients with <i>MED13L</i>-related intellectual disability highlighting the importance of genetic counseling. [PDF]

Front Genet
Cao H, He T, Wang J, Zhou C, Wei X, Zhang X.   +5 more
europepmc   +1 more source