New findings in a patient with distal 13q-

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.

Journal of medical genetics·2010

The beta-thalassemia mutation spectrum in the Iranian population.

Hemoglobin·2001

Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene.

Human mutation·2000

Supernumerary nipples in a Bartsocas-Papas patient in a consanguineous Iranian family.

Clinical dysmorphology·1999

An inappropriate erythropoietic response to iron deficiency anaemia in the elderly.

Clinical and laboratory haematology·1995

"Ultrahigh" dexamethasone in acute brain injury. Results from a prospective randomized double-blind multicenter trial (GUDHIS). German Ultrahigh Dexamethasone Head Injury Study Group.

Zentralblatt fur Neurochirurgie·1994

Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.

Clinical dysmorphology·2026

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

Clinical dysmorphology·2026

Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.

Clinical dysmorphology·2026

Identification of a novel mutation in metabotropic glutamate receptor 1 causing autosomal recessive spinocerebellar ataxia-13 in a Pakistani family.

Clinical dysmorphology·2026

Association between early repolarization and coronary slow flow phenomenon.

Cardiovascular revascularization medicine : including molecular interventions·2026

Added value of material decomposition for measuring brain calcification progression with spectral computed tomography in primary familial brain calcification.

European journal of radiology·2026

Unraveling Specific Binding Sites of Pulmonary Surfactants on the Coronavirus Spike Protein Receptor-Binding Domain.

The journal of physical chemistry. B·2026

Robust circular cluster-based statistics for respiration-brain coupling.

PLoS computational biology·2026

Standardized Spectral Mapping With 129Xe Chemical Shift Imaging: Investigating Red Blood Cell Shift Heterogeneity in Pulmonary Hypertension.

NMR in biomedicine·2026

Cough Hypersensitivity in Gastroesophageal Reflux-Induced Chronic Cough: Insights from Reflux Monitoring and High-Resolution Manometry.

Lung·2026

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New findings in a patient with distal 13q-

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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.

The beta-thalassemia mutation spectrum in the Iranian population.

Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene.

Supernumerary nipples in a Bartsocas-Papas patient in a consanguineous Iranian family.

An inappropriate erythropoietic response to iron deficiency anaemia in the elderly.

"Ultrahigh" dexamethasone in acute brain injury. Results from a prospective randomized double-blind multicenter trial (GUDHIS). German Ultrahigh Dexamethasone Head Injury Study Group.

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Added value of material decomposition for measuring brain calcification progression with spectral computed tomography in primary familial brain calcification.

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